Cas 279675-15-9,4(S)-benzyloxycarbonylamino-4-(methoxymethylcarbamoyl)butyric acid iso-butyl ester

279675-15-9

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Basic information

Product Name: 4(S)-benzyloxycarbonylamino-4-(methoxymethylcarbamoyl)butyric acid iso-butyl ester
Synonyms: 4(S)-benzyloxycarbonylamino-4-(methoxymethylcarbamoyl)butyric acid iso-butyl ester
CAS NO:279675-15-9
Molecular Formula:
Molecular Weight: 380.441
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: 4(S)-benzyloxycarbonylamino-4-(methoxymethylcarbamoyl)butyric acid iso-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4(S)-benzyloxycarbonylamino-4-(methoxymethylcarbamoyl)butyric acid iso-butyl ester(279675-15-9)
EPA Substance Registry System: 4(S)-benzyloxycarbonylamino-4-(methoxymethylcarbamoyl)butyric acid iso-butyl ester(279675-15-9)

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: 279675-15-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 279675-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,6,7 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 279675-15:
(8*2)+(7*7)+(6*9)+(5*6)+(4*7)+(3*5)+(2*1)+(1*5)=199
199 % 10 = 9
So 279675-15-9 is a valid CAS Registry Number.

279675-15-9Upstream product

6638-79-5 N,O-dimethylhydroxylamine*hydrochloride

279675-15-9Downstream Products

279675-17-1 4(S)-benzyloxycarbonylamino-5-oxo-pentanoic acid isobutyl ester

279675-15-9Relevant academic research and scientific papers

Synthesis of tetrahydro-β-carbolines and studies of the Pictet-Spengler reaction

Ducrot, Pierre,Rabhi, Cherif,Thal, Claude

, p. 2683 - 2692 (2000)

Tetrahydro-β-carbolines have been prepared in a diastereomerically pure form by a short, efficient synthetic sequence consisting of reaction of α- aminoaldehydes with tryptamine. A study was made of the major factors affecting the stereoselectivity of the

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