Cas 899442-11-6,{(R)-1-[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-carbamoyl]-but-3-enyl}-carbamic acid allyl ester

899442-11-6

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Basic information

Product Name: {(R)-1-[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-carbamoyl]-but-3-enyl}-carbamic acid allyl ester
Synonyms: {(R)-1-[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-carbamoyl]-but-3-enyl}-carbamic acid allyl ester
CAS NO:899442-11-6
Molecular Formula:
Molecular Weight: 346.426
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: {(R)-1-[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-carbamoyl]-but-3-enyl}-carbamic acid allyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(R)-1-[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-carbamoyl]-but-3-enyl}-carbamic acid allyl ester(899442-11-6)
EPA Substance Registry System: {(R)-1-[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-carbamoyl]-but-3-enyl}-carbamic acid allyl ester(899442-11-6)

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: 899442-11-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 899442-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,9,4,4 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 899442-11:
(8*8)+(7*9)+(6*9)+(5*4)+(4*4)+(3*2)+(2*1)+(1*1)=226
226 % 10 = 6
So 899442-11-6 is a valid CAS Registry Number.

899442-11-6Upstream product

899442-11-6Downstream Products

899442-18-3 Toluene-4-sulfonic acid (Z)-(R)-7-allyloxycarbonylamino-deca-5,9-dienyl ester

899442-11-6Relevant academic research and scientific papers

Antimalarial activity of a new family of analogues of manzamine A

Winkler, Jeffrey D.,Londregan, Allyn T.,Hamann, Mark T.

, p. 2591 - 2594 (2006)

Manzamine A represents an important lead structure for the development of novel antimalarial chemotherapies. The synthesis and biological evaluation of a group of simplified analogues of manzamine A, which were designed to examine the roles of the A and D

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