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Benzoic acid, 4,4'-[1,4-butanediylbis(iminocarbonyl)]bis-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102810-33-3

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102810-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102810-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102810-33:
(8*1)+(7*0)+(6*2)+(5*8)+(4*1)+(3*0)+(2*3)+(1*3)=73
73 % 10 = 3
So 102810-33-3 is a valid CAS Registry Number.

102810-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-[4-[(4-methoxycarbonylbenzoyl)amino]butylcarbamoyl]benzoate

1.2 Other means of identification

Product number -
Other names N,N'-Bis-(4-methoxycarbonyl-benzoyl)-tetramethylendiamin

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:102810-33-3 SDS

102810-33-3Relevant academic research and scientific papers

Synthesis and characterization of bis-and tris-(4-carboxybenzoyl)- alkaneamines

Guarda,Parra,Chavez,Belmar,Jimenez,Pasan,Ruiz-Perez

, p. 1305 - 1308 (2013/03/28)

A practical and efficient protocol to obtain bis- and tris-(4- carboxybenzoyl)alkaneamines based on monoprotected 1,4-benzenedicarboxylic acid is reported here. N-(4-methoxycarbonylbenzoyloxy)succinimide was treated with aliphatic diamines and triamines to form aliphatic hydrocarbon-linked bis- and tris-amides 4a-4e. The yields ranged from good to very good and showed that choosing the right acylating agent is a key point in this synthesis. All the compounds were characterized by elemental analysis, FTIR, and 1H NMR.

Stable amido peroxycarboxylic acids for bleaching

-

, (2008/06/13)

An amido peroxyacid compound is provided having the formula: STR1 wherein R is selected from the group consisting of C1 -C12 alkylene, C5 -C12 cycloalkylene, C6 -C12 arylene and radical combinations thereof; R1 and R2 are independently selected from the group consisting of H, C1 -C16 alkyl and C6 -C12 aryl radicals and a radical that can form a C3 -C12 ring together with R3 and both nitrogens; R3 is selected from the group consisting of C1 -C12 alkylene, C5 -C12 cycloalkylene and C6 -C12 arylene radicals, and provided when R3 is arylene and when n' and m' are each zero, R is other than C5 alkylene; n and n' each are an integer chosen such that the sum thereof is 1; m and m' each are an integer chosen such that the sum thereof is 1; and M is selected from the group consisting of H, alkali metal, alkaline earth metal, ammonium, alkanolammonium cations and radicals and combinations thereof. The amido peroxyacid compound is useful for bleaching substrates such as stained laundry.

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