Cas 635291-74-6,methyl (3S)-2-{(2S,3S)-3-cyclohexyl-2-[(trifluoroacetyl)amino]pent-4-enoyl}-1-benzyloxycarbonylpyrazolidine-3-carboxylate

635291-74-6

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Basic information

Product Name: methyl (3S)-2-{(2S,3S)-3-cyclohexyl-2-[(trifluoroacetyl)amino]pent-4-enoyl}-1-benzyloxycarbonylpyrazolidine-3-carboxylate
Synonyms:
CAS NO:635291-74-6
Molecular Formula:
Molecular Weight: 539.552
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: methyl (3S)-2-{(2S,3S)-3-cyclohexyl-2-[(trifluoroacetyl)amino]pent-4-enoyl}-1-benzyloxycarbonylpyrazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (3S)-2-{(2S,3S)-3-cyclohexyl-2-[(trifluoroacetyl)amino]pent-4-enoyl}-1-benzyloxycarbonylpyrazolidine-3-carboxylate(635291-74-6)
EPA Substance Registry System: methyl (3S)-2-{(2S,3S)-3-cyclohexyl-2-[(trifluoroacetyl)amino]pent-4-enoyl}-1-benzyloxycarbonylpyrazolidine-3-carboxylate(635291-74-6)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 635291-74-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 635291-74-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,5,2,9 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 635291-74:
(8*6)+(7*3)+(6*5)+(5*2)+(4*9)+(3*1)+(2*7)+(1*4)=166
166 % 10 = 6
So 635291-74-6 is a valid CAS Registry Number.

635291-74-6Upstream product

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635291-74-6Relevant academic research and scientific papers

Constrained peptidomimetics: Building bicyclic analogs of pyrazoline derivatives

Liu, Bin,Brandt, John D.,Moeller, Kevin D.

, p. 8515 - 8523 (2007/10/03)

A synthetic route has been developed for incorporating pyrazoline derivatives as proline surrogates in constrained X-Pro peptidomimetics. The route allows for the synthesis of dipeptide building blocks having either a six or seven-membered-ring annulated

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