Cas 161563-59-3,(2R,4S)-2-aminomethyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid diphenylmethyl ester

161563-59-3

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Basic information

Product Name: (2R,4S)-2-aminomethyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid diphenylmethyl ester
Synonyms: (2R,4S)-2-aminomethyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid diphenylmethyl ester
CAS NO:161563-59-3
Molecular Formula:
Molecular Weight: 356.489
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,4S)-2-aminomethyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid diphenylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4S)-2-aminomethyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid diphenylmethyl ester(161563-59-3)
EPA Substance Registry System: (2R,4S)-2-aminomethyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid diphenylmethyl ester(161563-59-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 161563-59-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161563-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,6 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 161563-59:
(8*1)+(7*6)+(6*1)+(5*5)+(4*6)+(3*3)+(2*5)+(1*9)=133
133 % 10 = 3
So 161563-59-3 is a valid CAS Registry Number.

161563-59-3Upstream product

908093-98-1 diazodiphenylmethane

161563-59-3Downstream Products

161563-59-3Relevant academic research and scientific papers

Synthesis of the first penicillin derivatives with medium-sized lactam ring and of related thiazolidines

Imming

, p. 207 - 215 (1995)

The novel concept of penicillin derivatives 4 with a medium-sized instead of a β-lactam ring is presented. Two synthetic paths were invented, resulting in the evaluation of the synthetic potential in the succinic, glutaric, and adipic acid series: A numbe

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