Cas 135356-94-4,2-tert-Butoxycarbonylamino-3-methyl-pent-4-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

135356-94-4

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Basic information

Product Name: 2-tert-Butoxycarbonylamino-3-methyl-pent-4-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Synonyms:
CAS NO:135356-94-4
Molecular Formula:
Molecular Weight: 443.627
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: 2-tert-Butoxycarbonylamino-3-methyl-pent-4-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-tert-Butoxycarbonylamino-3-methyl-pent-4-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(135356-94-4)
EPA Substance Registry System: 2-tert-Butoxycarbonylamino-3-methyl-pent-4-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(135356-94-4)

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: 135356-94-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135356-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,5 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 135356-94:
(8*1)+(7*3)+(6*5)+(5*3)+(4*5)+(3*6)+(2*9)+(1*4)=134
134 % 10 = 4
So 135356-94-4 is a valid CAS Registry Number.

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135356-94-4Relevant academic research and scientific papers

Enantioselective Syntheses of α-Amino Acids via Carbon-Carbon Bond Forming Radical Reactions

Hamon, David P. G.,Massy-Westropp, Ralph A.,Razzino, Pasquale

, p. 722 - 724 (1991)

The derivative of glycine, 8-phenylmenthyl N-Boc-2-bromoglycinate 2 reacts with unsaturated stannanes to give unsaturated amino acid derivatives with high diastereoselectivity.

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