Cas 201408-95-9,(S)-2-[(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-phenyl-propionylamino]-3-(3-trityl-3H-imidazol-4-yl)-propionic acid methyl ester

201408-95-9

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Basic information

Product Name: (S)-2-[(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-phenyl-propionylamino]-3-(3-trityl-3H-imidazol-4-yl)-propionic acid methyl ester
Synonyms: (S)-2-[(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-phenyl-propionylamino]-3-(3-trityl-3H-imidazol-4-yl)-propionic acid methyl ester
CAS NO:201408-95-9
Molecular Formula:
Molecular Weight: 706.841
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: (S)-2-[(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-phenyl-propionylamino]-3-(3-trityl-3H-imidazol-4-yl)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-phenyl-propionylamino]-3-(3-trityl-3H-imidazol-4-yl)-propionic acid methyl ester(201408-95-9)
EPA Substance Registry System: (S)-2-[(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-phenyl-propionylamino]-3-(3-trityl-3H-imidazol-4-yl)-propionic acid methyl ester(201408-95-9)

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: 201408-95-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201408-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,0 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 201408-95:
(8*2)+(7*0)+(6*1)+(5*4)+(4*0)+(3*8)+(2*9)+(1*5)=89
89 % 10 = 9
So 201408-95-9 is a valid CAS Registry Number.

201408-95-9Upstream product

201408-95-9Downstream Products

143072-03-1 (S)-3-(3H-Imidazol-4-yl)-2-((S)-2-methylamino-3-phenyl-propionylamino)-propionic acid methyl ester

201408-95-9Relevant academic research and scientific papers

The effects of N-methylation on the enantioselectivity of catalysis by cyclo[(R)-His-(R)-Phe]

Thoen, Jason C.,Lipton, Mark A.

, p. 3947 - 3954 (2007/10/03)

The cyclic dipeptide cyclo[(R)-His-(R)-Phe] 1 has been known since 1981 to catalyze the enantioselective formation of cyanohydrins from aldehydes and HCN. Although 1 has proved to be very effective in the production of optically active cyanohydrins, the p

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