Cas 1353744-36-1,phenylalanine-N-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamino)thioxomethyl]ethyl ester

1353744-36-1

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Basic information

Product Name: phenylalanine-N-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamino)thioxomethyl]ethyl ester
Synonyms: phenylalanine-N-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamino)thioxomethyl]ethyl ester
CAS NO:1353744-36-1
Molecular Formula:
Molecular Weight: 582.629
EINECS: N/A
Product Categories: N/A
Mol File: 1353744-36-1.mol
Article Data: 1

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: phenylalanine-N-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamino)thioxomethyl]ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: phenylalanine-N-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamino)thioxomethyl]ethyl ester(1353744-36-1)
EPA Substance Registry System: phenylalanine-N-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamino)thioxomethyl]ethyl ester(1353744-36-1)

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: 1353744-36-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1353744-36-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,7,4 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1353744-36:
(9*1)+(8*3)+(7*5)+(6*3)+(5*7)+(4*4)+(3*4)+(2*3)+(1*6)=161
161 % 10 = 1
So 1353744-36-1 is a valid CAS Registry Number.

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1353744-36-1Relevant articles and documents

Regioselective synthesis of novel 3-thiazolidine acetic acid derivatives from glycosido ureides

Li, Yuxin,Chen, Wei,Yang, Xiaoping,Yu, Guanping,Mao, Mingzhen,Zhou, Yunyun,Liu, Tuanwei,Li, Zhengming

, p. 969 - 978 (2011)

A series of 3-thiazolidine acetic acid-2-(per-O-acetylglycosyl)-1′-imino-α-(substituted)-4-oxo ethyl ester derivatives (3a-t) were prepared via the reaction of substituted amino acid-N-[(per-O-acetylglycosylamino)thioxomethyl]-ethyl ester with ethyl bromo

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