Cas 71610-01-0,(2R,3S)-2-Hydroxy-3-((E)-2-methyl-but-2-enoylamino)-3-phenyl-propionic acid methyl ester

71610-01-0

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Basic information

Product Name: (2R,3S)-2-Hydroxy-3-((E)-2-methyl-but-2-enoylamino)-3-phenyl-propionic acid methyl ester
Synonyms: (2R,3S)-2-Hydroxy-3-((E)-2-methyl-but-2-enoylamino)-3-phenyl-propionic acid methyl ester
CAS NO:71610-01-0
Molecular Formula:
Molecular Weight: 277.32
EINECS: N/A
Product Categories: N/A
Mol File: 71610-01-0.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: (2R,3S)-2-Hydroxy-3-((E)-2-methyl-but-2-enoylamino)-3-phenyl-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-2-Hydroxy-3-((E)-2-methyl-but-2-enoylamino)-3-phenyl-propionic acid methyl ester(71610-01-0)
EPA Substance Registry System: (2R,3S)-2-Hydroxy-3-((E)-2-methyl-but-2-enoylamino)-3-phenyl-propionic acid methyl ester(71610-01-0)

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: 71610-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 71610-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71610-01:
(7*7)+(6*1)+(5*6)+(4*1)+(3*0)+(2*0)+(1*1)=90
90 % 10 = 0
So 71610-01-0 is a valid CAS Registry Number.

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71610-01-0Relevant articles and documents

Anitleukemic Alkaloids from Taxus wallichiana Zucc.

Miller, Roger W.,Powell, Richard G.,Smith, Cecil R.

, p. 1469 - 1474 (2007/10/02)

A new antileukemic taxane alkaloid, cephalomannine (1a), has been isolated from leaves, stems, and roots of Taxus wallichiana Zucc.Cephalomannine is closely related to taxol (1b), a previously characterized antileukemic alkaloid, which also occurs in T. wallichiana but in lesser amounts than cephalomannine.The new alkaloid and its hydrolysis products were characterized by nuclear magnetic resonance, mass spetroscopy, and X-ray crystallography; taxol and two cytotoxic taxane congeners were also identified.

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