Molecule:100617
From ChemWiki
molecule
Properties | |
---|---|
CID | 996 |
CAS | 108-95-2 |
IUPAC-Name | phenol |
Abbreviation | PhOH |
Trivialname | phenol |
Exact mass | 94.041864811 |
Molecular formula | C6H6O |
LogP | 1.5 |
Has vendors | true |
Molecular role | n/a |
Synonyms | phenol, carbolic acid, Hydroxybenzene, Phenic acid, Oxybenzene, Phenylic acid, Phenylic alcohol, Benzenol, Monophenol, Phenyl hydrate, Phenyl hydroxide, PhOH, Monohydroxybenzene, Phenyl alcohol, Paoscle, Phenole, Izal, Phenol alcohol, Phenol, liquefied, Acide carbolique, Phenosmolin, Fenolo, Phenol homopolymer, Benzene, hydroxy-, Carbolsaure, Fenosmolin, Fenosmoline, Fenol, Liquid phenol, Carbolic oil, Liquefied phenol, Phenol, pure, [[Synonym::Fenolo [Italian]]], [[Synonym::Phenole [German]]], Rcra waste number U188, Campho-Phenique Gel, [[Synonym::Phenol [JAN]]], Phenic, [[Synonym::Carbolsaure [German]]], Campho-Phenique Liquid, NCI-C50124, Liquified Phenol, Phenol, molten, Baker's P & S liquid & Ointment, Carbolicum acidum, [[Synonym::Fenol [Dutch, Polish]]], Baker's P and S Liquid and Ointment, Monohydroxy benzene, Phenol, sulfurated, Un 2812 (solution), UN 2312 (molten), [[Synonym::Acide carbolique [French]]], UN 1671 (solid), NSC 36808, Campho-Phenique Cold Sore Gel, Anbesol, Phenic alcohol, Synthetic phenol, 2-allphenol, Phenol, dimer, RCRA waste no. U188, Phenol, liquified, MFCD00002143, UN1671, UN2312, UN2821, AI3-01814, NSC-36808, CHEMBL14060, 339NCG44TV, DTXSID5021124, CHEBI:15882, Phenol (or solutions with 5% or more phenol), ENT-1814, [[Synonym::Phenol, solid [UN1671] [Poison]]], [[Synonym::Phenol, molten [UN2312] [Poison]]], NCGC00091454-04, [[Synonym::Phenol solutions [UN2821] [Poison]]], DSSTox_CID_1124, Phenol, >=99.0%, DSSTox_RID_75955, DSSTox_GSID_21124, Caswell No. 649, phenylalcohol, hydroxy benzene, Phenol 100 microg/mL in Methanol, Phenol, liquid, Phenol, solid, Baker's p and s, CAS-108-95-2, CCRIS 504, FEMA No. 3223, HSDB 113, (14C)Phenol, [[Synonym::Phenol [USP:JAN]]], PHENOL (2,3,4,5,6-D5), EINECS 203-632-7, EPA Pesticide Chemical Code 064001, arenols, UNII-339NCG44TV, Benzophenol, Carbolsaeure, Karbolsaeure, Extracts, coal tar oil alk., acide phenique, Hydroxy-benzene, Phenol solution, Phenol liquid, Phenol molten, Phenol solutions, Phenol synthetic, Phenol,liquified, Phenolated water, Pandy's reagent, Cepastat lozenges, Phenol, labeled with carbon-14, Phenol (liquid), 2-phenyl alcohol, Phenol, synthetic, Phenol, ultrapure, Phenol ACS grade, EINECS 262-972-4, Paoscle (TN), Carbolic acid liquid, Phenol polymer-bound, Phenol (Granulated), Phenol (TN), Phenol,(S), Phenol, ACS reagent, Carbolic acid, liquid, 1ai7, 1li2, 4i7l, Liquefied phenol (TN), [[Synonym::PHENOL [VANDF]]], [[Synonym::PHENOL [FHFI]]], [[Synonym::PHENOL [HSDB]]], [[Synonym::PHENOL [IARC]]], [[Synonym::PHENOL [INCI]]], Phenol (JP17/USP), [[Synonym::PHENOL [USP-RS]]], [[Synonym::PHENOL [WHO-DD]]], Phenol, detached crystals, [[Synonym::PHENOL [II]]], [[Synonym::PHENOL [MI]]], Phenol, >=99%, [[Synonym::PHENOL [MART.]]], WLN: QR, Liquefied phenol (JP17), bmse000290, bmse010026, C6H5OH, Fenol(DUTCH, POLISH), EC 203-632-7, PHENOL, 80% in ethanol, Phenol, LR, >=99%, MLS001065591, Phenol, for molecular biology, BIDD:ER0293, [[Synonym::PHENOL [EP MONOGRAPH]]], Phenol for disinfection (TN), Phenol, natural, 97%, FG, [[Synonym::PHENOL [USP MONOGRAPH]]], Cuticura pain relieving ointment, [[Synonym::CARBOLICUM ACIDUM [HPUS]]], Phenol, AR, >=99.5%, [[Synonym::PHENOL,LIQUIFIED [VANDF]]], BDBM26187, CHEBI:33853, Phenol for disinfection (JP17), Phenolated water for disinfection, Salicylic acid related compound c, 3f39, Phenol 10 microg/mL in Methanol, Phenol solution, 1.0 M in THF, NSC36808, ZINC5133329, Phenol, Glass Distilled Under Argon, Tox21_113463, Tox21_201639, Tox21_300042, Phenol 5000 microg/mL in Methanol, [[Synonym::phenol;phenol [jan];phenol, pure;phenol phenol [jan] phenol, pure]], STL194294, AKOS000119025, Tox21_113463_1, DB03255, NA 2821, Phenol, BioXtra, >=99.5% (GC), Phenol, SAJ first grade, >=98.0%, UN 1671, UN 2312, UN 2821, NCGC00091454-01, NCGC00091454-02, NCGC00091454-03, NCGC00091454-05, NCGC00091454-06, NCGC00091454-07, NCGC00254019-01, NCGC00259188-01, Phenol solution, 1 M in dichloromethane, Phenol, JIS special grade, >=99.0%, AM802906, BP-30160, [[Synonym::METHYL SALICYLATE IMPURITY B [EP]]], SMR000568492, Phenol 1000 microg/mL in Dichloromethane, Phenol, PESTANAL(R), analytical standard, Liquified Phenol (contains 7-10 % water), [[Synonym::METACRESOL IMPURITY A [EP IMPURITY]]], FT-0645154, FT-0673707, FT-0693833, P1610, P2771, Phenol stock solution, 100 mg/dL, standard, C00146, D00033, Phenol, unstabilized, ReagentPlus(R), >=99%, [[Synonym::SALICYLIC ACID IMPURITY C [EP IMPURITY]]], [[Synonym::HEXYLRESORCINOL IMPURITY A [EP IMPURITY]]], Phenol, p.a., ACS reagent, 99.5-100.5%, Phenol, >=96.0% (calc. on dry substance, T), Q130336, J-610001, Phenol, for molecular biology, ~90% (T), liquid, F1908-0106, Phenol, unstabilized, purified by redistillation, >=99%, [[Synonym::SALICYLIC ACID RELATED COMPOUND C [USP IMPURITY]]], Phenol, BioUltra, for molecular biology, >=99.5% (GC), Phenol, United States Pharmacopeia (USP) Reference Standard, Liquified Phenol, meets USP testing specifications, >=89.0%, Phenol, BioUltra, for molecular biology, TE-saturated, ~73% (T), Phenol solution, 5000 mug/mL in methanol, certified reference material, Phenol solution, certified reference material, 500 mug/mL in methanol, Phenol, puriss. p.a., ACS reagent, reag. Ph. Eur., 99.0-100.5%, p-Hydroxy polystyrene (100-200 mesh, 0.5-1.5 mmol/g)@CRLFMFCD03703209, Phenol solution, 100 mug/mL in acetonitrile, PESTANAL(R), analytical standard, Phenol, contains hypophosphorous as stabilizer, loose crystals, ACS reagent, >=99.0%, Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (GC), Phenol solution, BioReagent, Equilibrated with 10??mM Tris HCl, pH??8.0, 1??mM EDTA, for molecular biology, Phenol solution, BioReagent, Saturated with 0.1 M citrate buffer, pH??4.3 +/- 0.2, for molecular biology, Phenol, polymer-bound, 100-200 mesh, extent of labeling: 0.5-1.5 mmol/g loading, 1 % cross-linked with divinylbenzene, Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, >=99.5% (GC), crystalline (detached) |
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Molecule is used on following pages
topic
publication
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Photocatalytic CO2 Reduction Mediated by Electron Transfer via the Excited Triplet State of Zn(II) Porphyrin
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction
investigation
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions error
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Co catalyst testing
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/testtest2
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results obtained with Co2+ catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/results CO2+ experiments
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2+ results from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results Co2+ experiments taken from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2 Reduction under diverse conditions with diverse sensitizers