Cas 191422-05-6,(S)-3-Benzyloxycarbonylamino-N-((R)-1-methoxycarbonyl-1-phenyl-ethyl)-succinamic acid tert-butyl ester

191422-05-6

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Basic information

Product Name: (S)-3-Benzyloxycarbonylamino-N-((R)-1-methoxycarbonyl-1-phenyl-ethyl)-succinamic acid tert-butyl ester
Synonyms: (S)-3-Benzyloxycarbonylamino-N-((R)-1-methoxycarbonyl-1-phenyl-ethyl)-succinamic acid tert-butyl ester
CAS NO:191422-05-6
Molecular Formula:
Molecular Weight: 484.549
EINECS: N/A
Product Categories: N/A
Mol File: 191422-05-6.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: (S)-3-Benzyloxycarbonylamino-N-((R)-1-methoxycarbonyl-1-phenyl-ethyl)-succinamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-Benzyloxycarbonylamino-N-((R)-1-methoxycarbonyl-1-phenyl-ethyl)-succinamic acid tert-butyl ester(191422-05-6)
EPA Substance Registry System: (S)-3-Benzyloxycarbonylamino-N-((R)-1-methoxycarbonyl-1-phenyl-ethyl)-succinamic acid tert-butyl ester(191422-05-6)

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: 191422-05-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 191422-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,4,2 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 191422-05:
(8*1)+(7*9)+(6*1)+(5*4)+(4*2)+(3*2)+(2*0)+(1*5)=116
116 % 10 = 6
So 191422-05-6 is a valid CAS Registry Number.

191422-05-6Upstream product

29738-09-8 (R)-2-amino-2-phenylpropanoic acid

191422-05-6Downstream Products

191422-06-7 (S)-3-Benzyloxycarbonylamino-N-((R)-1-methoxycarbonyl-1-phenyl-ethyl)-succinamic acid

191422-05-6Relevant articles and documents

Aspartame dipeptide analogues: Effect of number of side-chain methylene group spacers and C(α)-methylation in the second position

Mossel, Eric,Formaggio, Fernando,Crisma, Marco,Toniolo, Claudio,Broxterman, Quirinus B.,Boesten, Wilhelmus H.J.,Kamphuis, Johan,Quaedflieg, Peter J.L.M.,Temussi, Piero

, p. 1305 - 1314 (1997)

Our model of the active site of the sweet taste receptor is shown to be consistent with the aspartame analogues in which the L-Phe2 residue is replaced by L-(αMe)Phg, L-(αMe)Phe or L-(αMe)Hph. The analogues containing either the first or the th

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