Cas 120226-01-9,5-Benzyloxy-5-hydroxy-3-phenyl-[1,2,4]triazolidine-1,2,3-tricarboxylic acid 1,2-diisopropyl ester 3-methyl ester

120226-01-9

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Basic information

Product Name: 5-Benzyloxy-5-hydroxy-3-phenyl-[1,2,4]triazolidine-1,2,3-tricarboxylic acid 1,2-diisopropyl ester 3-methyl ester
Synonyms:
CAS NO:120226-01-9
Molecular Formula:
Molecular Weight: 501.536
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: 5-Benzyloxy-5-hydroxy-3-phenyl-[1,2,4]triazolidine-1,2,3-tricarboxylic acid 1,2-diisopropyl ester 3-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-Benzyloxy-5-hydroxy-3-phenyl-[1,2,4]triazolidine-1,2,3-tricarboxylic acid 1,2-diisopropyl ester 3-methyl ester(120226-01-9)
EPA Substance Registry System: 5-Benzyloxy-5-hydroxy-3-phenyl-[1,2,4]triazolidine-1,2,3-tricarboxylic acid 1,2-diisopropyl ester 3-methyl ester(120226-01-9)

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: 120226-01-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120226-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,2 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 120226-01:
(8*1)+(7*2)+(6*0)+(5*2)+(4*2)+(3*6)+(2*0)+(1*1)=59
59 % 10 = 9
So 120226-01-9 is a valid CAS Registry Number.

120226-01-9Upstream product

120226-01-9Downstream Products

120226-01-9Relevant academic research and scientific papers

OXIDATIONS OF SOME α-AMINO ACIDS UNDER MITSUNOBU REACTION CONDITIONS

Kolasa, Teodozyj,Miller, Marvin J.

, p. 4661 - 4664 (1988)

Reactions of α-amino acids with azodicarboxylates and Ph3P results in oxidation at the α-carbon.N-acyl or carbamoyl amino acid esters give azodicarboxylate adducts, whereas free α-amino acid esters are converted to the corresponding α-keto esters.

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