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2,5-Pyrrolidinedione, 1-[[4-(chlorodiphenylmethyl)benzoyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

164168-40-5

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164168-40-5 Usage

Molecular weight

315.76 g/mol

Chemical structure

2,5-Pyrrolidinedione, 1-[[4-(chlorodiphenylmethyl)benzoyl]oxy]-

Type of compound

Ester of chlorphenesin and carbamic acid

Uses

Muscle relaxant in cosmetic and personal care products, preservative in various formulations, and in certain medical treatments for muscle spasms and wrinkles

Mechanism of action

Inhibits the release of acetylcholine at the neuromuscular junction, leading to muscle relaxation

Precautions

Should be handled carefully and used only as directed to avoid skin irritation and other adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 164168-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,1,6 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 164168-40:
(8*1)+(7*6)+(6*4)+(5*1)+(4*6)+(3*8)+(2*4)+(1*0)=135
135 % 10 = 5
So 164168-40-5 is a valid CAS Registry Number.

164168-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dioxopyrrolidin-1-yl) 4-[chloro(diphenyl)methyl]benzoate

1.2 Other means of identification

Product number -
Other names 2,5-Pyrrolidinedione,1-[[4-(chlorodiphenylmethyl)benzoyl]oxy]

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:164168-40-5 SDS

164168-40-5Relevant academic research and scientific papers

Trityl tags for encoding in combinatorial synthesis

Shchepinov, Mikhail S.,Chalk, Rod,Southern, Edwin M.

, p. 2713 - 2724 (2000)

New tags and an encoding strategy for combinatorial synthesis are described. Combinatorial libraries of short oligonucleotides attached to TentaGel beads were synthesised by a split-and-mix strategy using 5'-DMTr or 5'-Fmoc-protected nucleoside phosphoramidites. Trityl moieties with different masses were used to tag the nature and position of monomer units (bases) coupled at each step in the synthesis. Beads with a specific oligonucleotide were selected by hybridisation from combinatorial libraries. Tags orthogonal to the added nucleotides were produced by coupling amines of different molecular masses to an activated carboxyl group(s) on the trityl moiety. The tags may be released from the support by an acidic treatment or laser irradiation and then analysed by (MA)LDI-TOF. These properties make trityl- based tags promising for encoding in strategies not involving strong acids, such as oligonucleotide and peptide synthesis and small molecule combinatorial libraries. (C) 2000 Published by Elsevier Science Ltd.

Acid labile immunoconjugate intermediates

-

, (2008/06/13)

Trityl derivatives useful as "linkers" for preparation of imunoconjugates comprising drugs end antibodies are provided. Immunoconjugates and processes for their preparation and use are also provided. This invention also provides for prodrugs comprising a

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