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37055-79-1

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37055-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37055-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,5 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37055-79:
(7*3)+(6*7)+(5*0)+(4*5)+(3*5)+(2*7)+(1*9)=121
121 % 10 = 1
So 37055-79-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-15-13-9-11(7-8-12(13)14)10-5-3-2-4-6-10/h2-9,14H,1H3

37055-79-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-4-phenylphenol

1.2 Other means of identification

Product number -
Other names 3-methoxy-4-biphenylol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37055-79-1 SDS

37055-79-1Downstream Products

37055-79-1Relevant articles and documents

An expeditious aqueous Suzuki-Miyaura method for the arylation of bromophenols

Freundlich, Joel S.,Landis, Howard E.

, p. 4275 - 4279 (2007/10/03)

The development of a novel Suzuki-Miyaura method has been achieved to allow the efficient arylation of bromophenols. A range of functionality is tolerated with regard to the boronic acid coupling partner and the reaction exhibits complete chemoselectivity for the Caryl-Br bond versus the Caryl-Cl bond in the aryl halide input. The experimental protocol features a short reaction time of 15 min, utilizes inexpensive Pd/C as a catalyst, and is conducted with water as the solvent.

WB4101-related compounds: New, subtype-selective α1- adrenoreceptor antagonists (or inverse agonists?)

Pallavicini, Marco,Budriesi, Roberta,Fumagalli, Laura,Ioan, Pierfranco,Chiarini, Alberto,Bolchi, Cristiano,Ugenti, Maria Paola,Colleoni, Simona,Gobbi, Marco,Valoti, Ermanno

, p. 7140 - 7149 (2007/10/03)

Our previous structure-affinity relationship study had considered the enantiomers of the naphthodioxane, tetrahydronaphthodioxane, and 2-methoxy-1-naphthoxy analogues (compounds 1, 3, and 2, respectively) of 2-(2,6-dimethoxyphenoxyethylaminomethyl)-1,4-be

A NEW ENTRY TO 1,2-BENZENEDIOL CONGENERS

Ozaki, Yutaka,Oshio, Ikumi,Kim, Sang-Won

, p. 1434 - 1436 (2007/10/02)

1,2-Benzenediols and their monoethers were efficiently prepared from α,α-bis(ethylthio)cyclohexenones which were constructed by the C3+C3 annulation of 1,1-bis(ethylthio)propan-2-one and the Mannich bases. KEYWORDS 1,2-benzenediol; aromatic synthesis; annulation; aromatic compound; acetal

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