16045-92-4 Usage
Description
CHLOROSUCCINIC ACID, also known as 2-chlorosuccinic acid, is a C4-dicarboxylic acid that is succinic acid substituted at position 2 by a chloro group. It is a chemical compound with potential applications in various industries due to its unique properties.
Uses
Used in Chemical Synthesis:
CHLOROSUCCINIC ACID is used as a building block for the synthesis of various organic compounds, particularly in the pharmaceutical and chemical industries. Its unique structure allows for the creation of a wide range of products, making it a versatile starting material.
Used in Pharmaceutical Industry:
CHLOROSUCCINIC ACID is used as an intermediate in the production of certain pharmaceuticals, such as antibiotics and other therapeutic agents. Its reactivity and ability to form derivatives make it a valuable component in the development of new drugs.
Used in Dye and Pigment Industry:
In the dye and pigment industry, CHLOROSUCCINIC ACID is used as a key component in the synthesis of various dyes and pigments. Its chemical properties enable the creation of a diverse range of colors and shades, contributing to the production of high-quality dyes and pigments.
Used in Agricultural Industry:
CHLOROSUCCINIC ACID is also utilized in the agricultural industry, where it serves as a starting material for the synthesis of certain agrochemicals, such as herbicides and pesticides. Its role in the development of these products helps to improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 16045-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,4 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16045-92:
(7*1)+(6*6)+(5*0)+(4*4)+(3*5)+(2*9)+(1*2)=94
94 % 10 = 4
So 16045-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H5ClO3/c5-3(6)1-2-4(7)8/h1-2H2,(H,7,8)
16045-92-4Relevant articles and documents
-
Pudovik,A.N. et al.
, (1966)
-
-
Gawron,O. et al.
, p. 3877 - 3882 (1962)
-
TOTAL SYNTHESIS OF ANTITUMOR AGENT AT-125, (αS,5S)-α-AMINO-3-CHLORO-4,5-DIHYDRO-5-ISOXAZOLEACETIC ACID
Baldwin, Jack E.,Cha, Jin K.,Kruse, Lawrence I.
, p. 5241 - 5260 (2007/10/02)
A short and efficient total synthesis of racemic AT-125 and its racemic threo isomer proceeds via an intramolecular Michael cyclization of a protected α,β-dehydroglutamic acid γ-hydroxamate.Separation of diastereomers and deprotection to racemic AT-125 followed by enzymatic resolution of the N-chloroacetamide with hog-kidney acylase provides the natural αS,5S isomer.
