Cas 134210-48-3,(E)-(2S,5S)-5-tert-Butoxycarbonylamino-2-isopropyl-6-phenyl-hex-3-enoic acid methyl ester

134210-48-3

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Basic information

Product Name: (E)-(2S,5S)-5-tert-Butoxycarbonylamino-2-isopropyl-6-phenyl-hex-3-enoic acid methyl ester
Synonyms: (E)-(2S,5S)-5-tert-Butoxycarbonylamino-2-isopropyl-6-phenyl-hex-3-enoic acid methyl ester
CAS NO:134210-48-3
Molecular Formula:
Molecular Weight: 361.481
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: (E)-(2S,5S)-5-tert-Butoxycarbonylamino-2-isopropyl-6-phenyl-hex-3-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(2S,5S)-5-tert-Butoxycarbonylamino-2-isopropyl-6-phenyl-hex-3-enoic acid methyl ester(134210-48-3)
EPA Substance Registry System: (E)-(2S,5S)-5-tert-Butoxycarbonylamino-2-isopropyl-6-phenyl-hex-3-enoic acid methyl ester(134210-48-3)

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: 134210-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134210-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,1 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134210-48:
(8*1)+(7*3)+(6*4)+(5*2)+(4*1)+(3*0)+(2*4)+(1*8)=83
83 % 10 = 3
So 134210-48-3 is a valid CAS Registry Number.

134210-48-3Upstream product

127882-33-1 (E)-(4S,5S)-5-tert-Butoxycarbonylamino-4-methanesulfonyloxy-6-phenyl-hex-2-enoic acid methyl ester

134210-48-3Downstream Products

134210-48-3Relevant academic research and scientific papers

A Highly Stereoselective Synthesis of (E)-Alkene Dipeptide Isosteres via Organocyanocopper-Lewis Acid Mediated Reaction

Ibuka, Toshiro,Habashita, Hiromu,Otaka, Akira,Fujii, Nobutaka,Oguchi, Yusaku,Uyehara, Tadao et al.

, p. 4370 - 4382 (2007/10/02)

A stereoselective synthesis of protected (E)-alkene dipeptide isosteres by the reaction of the mesylates of homochiral δ-aminated γ-hydroxy (E)-α,β-enoates with either RCu(CN)Li-BF3 or RCu(CN)MgX.BF3 reagent is described.The degree of diastereoselectivity

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