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Bis(MethoxycarbonylaMino)acetic acid, also known as N,N'-bis-(methoxycarbonyl)glycine, is a chemical compound with the molecular formula C6H9NO7. It is a derivative of the amino acid glycine and is commonly recognized for its chelating properties.

110599-27-4

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110599-27-4 Usage

Uses

Used in Industrial Applications:
Bis(MethoxycarbonylaMino)acetic acid is used as a chelating agent for the production of metal chelates and metal ion sequestration. It has a high affinity for metal ions such as copper, zinc, and nickel, effectively sequestering these ions to prevent interference in processes like dyeing, metal finishing, and water treatment.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Bis(MethoxycarbonylaMino)acetic acid serves as a precursor in the synthesis of potential drug candidates, contributing to the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 110599-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,9 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110599-27:
(8*1)+(7*1)+(6*0)+(5*5)+(4*9)+(3*9)+(2*2)+(1*7)=114
114 % 10 = 4
So 110599-27-4 is a valid CAS Registry Number.

110599-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis[(methoxycarbonyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names bismethoxycarbonylaminoacetic 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:110599-27-4 SDS

110599-27-4Relevant academic research and scientific papers

INTRA VS INTERMOLECULAR AMIDOALKILATION OF AROMATICS

Ishai, D. Ben,Sataty, I.,Peled, N.,Goldshare, R.

, p. 439 - 450 (2007/10/02)

Three tipes of intramolecular amidoalkylation reactions of aromatics, two endotrigonal and one exotrigonal (I, II, III), leading to indolone, N-acylisoquinolines, isoquinolone and benzazepinone derivatives were studied.In the presence of external aromatic nucleophiles competing intermolecular amidoalkylations were observed (1->2, 13->14).The mechanism and the synthetic limitations of the three types of cyclization is discussed.

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