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6997-34-8

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6997-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6997-34-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,9 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6997-34:
(6*6)+(5*9)+(4*9)+(3*7)+(2*3)+(1*4)=148
148 % 10 = 8
So 6997-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O3/c1-3-8(11)7-4-5-9(12)10(6-7)13-2/h4-6,8,11-12H,3H2,1-2H3

6997-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1-hydroxypropyl)-2-methoxyphenol

1.2 Other means of identification

Product number -
Other names -

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:6997-34-8 SDS

6997-34-8Relevant articles and documents

Specific features of solvation of lignin related phenols in the binary mixtures of water with dimethyl sulfoxide, 1,4-dioxane, and acetonitrile

Kosyakov,Bogolitsyn,Gorbova

, p. 2045 - 2050 (2014)

The effect of the solvent composition in the binary mixtures of water with dimethyl sulfoxide, acetonitrile and 1,4-dioxane on the positions of absorption bands in the UV spectra of five guaiacylic phenols, as well as of the corresponding phenolate anions

A novel synthesis of isoeugenol, [ring-(U)-14C]

Immoos, John E.

, p. 419 - 424 (2015/11/18)

A novel method for the preparation of isoeugenol, [ring-(U)-14C] is presented. Phenols and phenyl esters substituted in the para position with 1-hydroxyethyl or 1-hydroxypropyl acetate esters when treated with 1,8-diazabicyclo[5.4.0]undec-7-ene in dimethylformamide (DMF) eliminate the alkyl carboxylate function to give the unsaturated compound. The reaction fails with unsubstituted or ether substituted phenyl 1-hydroxyacetate esters.

Synthesis of 1,2-dihydronaphthalenes and spiro[4.5]-deca-3,6,9-trien-8-ones from benzylic alcohols

Angle,Arnaiz

, p. 2327 - 2330 (2007/10/02)

The synthesis of 1,2-dihydronaphthalenes and spiro[4.5]decatrienones via reaction of an allenyl-silane and a benzylic cation is reported.

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