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1035202-87-9

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1035202-87-9 Usage

Classification

Organic acid

Common uses

Synthesis of pharmaceuticals, agrochemicals, and other fine chemicals

Potential applications

Intermediate in the production of various pharmaceuticals and agrochemicals

Structure

Acetate ester of 2-phenyl-2-propyl glycolic acid

Possible future applications

Novel applications in medicine and agriculture

Research and development importance

Further investigation into its potential uses and properties could lead to new discoveries and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1035202-87-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,2,0 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1035202-87:
(9*1)+(8*0)+(7*3)+(6*5)+(5*2)+(4*0)+(3*2)+(2*8)+(1*7)=99
99 % 10 = 9
So 1035202-87-9 is a valid CAS Registry Number.

1035202-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-methyl-1-phenylethoxy)acetic acid

1.2 Other means of identification

Product number -
Other names (1-methyl-1-phenyl-ethoxy)-acetic acid

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:1035202-87-9 SDS

1035202-87-9Relevant articles and documents

Lewis base activation of Lewis acids: Catalytic, enantioselective addition of glycolate-derived silyl ketene acetals to aldehydes

Denmark, Scott E.,Chung, Won-Jin

, p. 4582 - 4595 (2008/09/21)

(Chemical Equation Presented) A catalytic system involving silicon tetrachloride and a chiral, Lewis basic bisphosphoramide catalyst is effective for the addition of glycolate-derived silyl ketene acetals to aldehydes. It was found that the sense of diast

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