33646-31-0 Usage
Uses
Used in Organic Synthesis:
D,L-3-CHLOROALANINE METHYL ESTER HYDROCHLORIDE is used as a synthetic building block for the development of complex organic molecules and pharmaceuticals. Its unique chemical structure allows for the formation of a wide range of compounds, making it a valuable asset in the field of organic chemistry.
Used in Pharmaceutical Industry:
D,L-3-CHLOROALANINE METHYL ESTER HYDROCHLORIDE is used as an intermediate in the synthesis of various pharmaceutical compounds. Its versatility in organic synthesis enables the creation of new drugs with potential therapeutic applications, contributing to the advancement of the pharmaceutical industry.
Used in Research and Development:
In the research and development sector, D,L-3-CHLOROALANINE METHYL ESTER HYDROCHLORIDE is employed as a key compound for exploring new chemical reactions and understanding the underlying mechanisms. This knowledge can be applied to develop innovative synthetic methods and improve existing ones, ultimately leading to the discovery of novel compounds with potential applications in various industries.
Used in Chemical Industry:
D,L-3-CHLOROALANINE METHYL ESTER HYDROCHLORIDE is used as a raw material in the chemical industry for the production of various specialty chemicals. Its unique properties make it suitable for the synthesis of compounds used in different applications, such as agrochemicals, dyes, and other industrial products.
Check Digit Verification of cas no
The CAS Registry Mumber 33646-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,4 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33646-31:
(7*3)+(6*3)+(5*6)+(4*4)+(3*6)+(2*3)+(1*1)=110
110 % 10 = 0
So 33646-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H8ClNO2/c1-8-4(7)3(6)2-5/h3H,2,6H2,1H3/t3-/m0/s1
33646-31-0Relevant academic research and scientific papers
Synthesis of N-acetyl-S-(3-coumarinyl)-cysteine methyl ester and HPLC analysis of urinary coumarin metabolites
Eisenbrand, Gerhard,Otteneder, Michael,Tang, Weici
, p. 249 - 258 (2008/01/27)
N-Acetyl-S-(3-coumarinyl)cysteine, a metabolite of coumarin in rodents, has been synthesized as methyl ester. A new synthetic route to prepare N-acetyl-S-(3-coumarinyl)-D,L-cysteine methyl ester (1) comprises reaction of 3-mercaptocoumarin (3) with N-acetyl-3-chloro-D,L-alanine methyl ester (4). N-acetyl-S-(4-coumarinyl)-L-cysteine (10) was obtained by reaction of 3-bromocoumarin (12) and N-acetyl-L-cysteine (13). A method for the determination of N-acetyl-S-(3-coumarinyl)cysteine as its methyl ester in urine by HPLC has been developed.
Synthesis of a Phosphinic Acid Transition State Analogue Inhibitor of Dihydroorotase
Cao, Yu,Christopherson, Richard I.,Elix, John A.,Gaul, Kim L.
, p. 903 - 912 (2007/10/02)
The synthesis of the phosphinic acid 4-hydroxy-6-oxo-1,4-azaphosphinane-2-carboxylic acid 4-oxide (11) is described.The phosphinic acid (11) was designed as a transition state analogue inhibitor of dihydroorotase.
