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127413-58-5

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127413-58-5 Usage

Usage

Plasticizer in the manufacturing of vinyl flooring, synthetic leather, and adhesives

Function

Increases flexibility, durability, and resistance to heat and cold in plastics

Health concerns

Potential endocrine-disrupting properties

Environmental impact

May be harmful to human health and the environment

Current focus

Finding alternative plasticizers that are safer and more environmentally friendly

Check Digit Verification of cas no

The CAS Registry Mumber 127413-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,1 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127413-58:
(8*1)+(7*2)+(6*7)+(5*4)+(4*1)+(3*3)+(2*5)+(1*8)=115
115 % 10 = 5
So 127413-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H13BrO4/c1-3-16-11(14)8-6-5-7-9(13)10(8)12(15)17-4-2/h5-7H,3-4H2,1-2H3

127413-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 3-bromobenzene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1,2-Benzenedicarboxylicacid,3-bromo-,1,2-diethyl ester

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:127413-58-5 SDS

127413-58-5Relevant articles and documents

Metallo-β-lactamase inhibitory activity of phthalic acid derivatives

Hiraiwa, Yukiko,Morinaka, Akihiro,Fukushima, Takayoshi,Kudo, Toshiaki

scheme or table, p. 5162 - 5165 (2010/03/24)

4-Butyl-3-methylphthalic acid was recognized as a metallo-β-lactamase inhibitor. The structure-activity relationship study of substituted phthalic acids afforded 3-phenylphthalic acid derivatives as potent IMP-1 inhibitors. On the other hand, 3-substituted with 4-hydroxyphenyl phthalic acid derivative displayed a potent combination effect with biapenem (BIPM) against Pseudomonas aeruginosa that produce IMP-1.

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