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77712-29-9

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77712-29-9 Usage

Chemical category

Alcohols

Carbon chain length

10-carbon chain

Functional group

Hydroxy group (-OH)

Type of alcohol

Primary alcohol

Aromatic nature

Phenyl ring with dimethoxy and methyl substituents

Hydroxy group position

Attached to the 2nd carbon of the phenyl ring

Dimethoxy substituents

Two methoxy groups (-OCH3) on the 3rd and 4th positions of the phenyl ring

Methyl substituent

One methyl group (-CH3) on the 6th position of the phenyl ring

Potential applications

Pharmaceutical or cosmetic industries

Research necessity

Further research and testing required to determine specific uses and potential benefits

Check Digit Verification of cas no

The CAS Registry Mumber 77712-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,1 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77712-29:
(7*7)+(6*7)+(5*7)+(4*1)+(3*2)+(2*2)+(1*9)=149
149 % 10 = 9
So 77712-29-9 is a valid CAS Registry Number.

77712-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(10-hydroxydecyl)-5,6-dimethoxy-3-methylphenol

1.2 Other means of identification

Product number -
Other names Benzenedecanol,2-hydroxy-3,4-dimethoxy-6-methyl

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:77712-29-9 SDS

77712-29-9Downstream Products

77712-29-9Relevant articles and documents

Reduction of carboxylic esters

-

, (2008/06/13)

A method for producing a compound of the formula: STR1 [wherein R1 and R2 each stand for a lower alkyl group; n denotes an integer of 0 to 21; X stands for hydrogen atom or an optionally protected hydroxyl group; and Y stands for an optionally protected hydroxyl group], which comprises reducing an ester compound of the formula: STR2 [wherein R1, R2, n, X and Y are of the same meaning as defined above, and R3 stands for a lower alkyl group ] with a mixture of sodium borohydride and aluminum chloride. This method give the desired compound in a high yield, and is advantageous from the industrial point of view.

Synthesis of quinones having carboxy- and hydroxy-alkyl side chains, and their effects on rat-liver lysosomal membrane.

Okamoto,Watanabe,Kawada,Goto,Ashida,Oda,Yajima,Imada,Morimoto

, p. 2797 - 2819 (2007/10/02)

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