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107188-34-1

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107188-34-1 Usage

Structure

Chroman ring with specific substituents
Consists of a chroman ring structure with four methyl groups (2,5,7,8-positions), a 4-nitrophenoxymethyl group, and an acetate group.

Usage

Research and development, pharmaceutical industry
Commonly used in the creation of novel drugs and medications, as well as a valuable tool in studying chemical and biological processes.

Potential applications

Drug candidate
Due to its unique structure and properties, it may have potential applications as a drug candidate.

Handling precautions

Caution advised
Due to its complexity and potential reactivity, it is important to exercise caution when handling and using this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 107188-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,8 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107188-34:
(8*1)+(7*0)+(6*7)+(5*1)+(4*8)+(3*8)+(2*3)+(1*4)=121
121 % 10 = 1
So 107188-34-1 is a valid CAS Registry Number.

107188-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,5,7,8-tetramethyl-2-[(4-nitrophenoxy)methyl]-4-oxo-3H-chromen-6-yl] acetate

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:107188-34-1 SDS

107188-34-1Relevant articles and documents

THIAZOLIDINE DERIVATIVES, THEIR PREPARATION AND USE

-

, (2008/06/13)

Compounds of formula (I): (in which R1-R7 are hydrogen or various organic groups, n is 1-10, Ar is an aromatic group, U is CH2 or a carbon atom doubly bonded to either one of its adjacent carbons, and W is >CH2, >C=0 , >CHOH, >C=NOH or various derivatives thereof) have the ability to lower the levels of blood lipid peroxides and blood sugars and to inhibit the activity of aldose reductase; they may be used therapeutically for these purposes.

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