Cas 478239-50-8,methyl (2S)-cis-(Z)-1-(tert-butyloxycarbonyl)-5-[2'-(4-methoxy-phenyl)-(3'-amino-(N-benzyloxycarbonyl)-3'-methoxycarbonyl)-2'-propenyl] prolinate

478239-50-8

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Basic information

Product Name: methyl (2S)-cis-(Z)-1-(tert-butyloxycarbonyl)-5-[2'-(4-methoxy-phenyl)-(3'-amino-(N-benzyloxycarbonyl)-3'-methoxycarbonyl)-2'-propenyl] prolinate
Synonyms: methyl (2S)-cis-(Z)-1-(tert-butyloxycarbonyl)-5-[2'-(4-methoxy-phenyl)-(3'-amino-(N-benzyloxycarbonyl)-3'-methoxycarbonyl)-2'-propenyl] prolinate
CAS NO:478239-50-8
Molecular Formula:
Molecular Weight: 582.651
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 (2S)-cis-(Z)-1-(tert-butyloxycarbonyl)-5-[2'-(4-methoxy-phenyl)-(3'-amino-(N-benzyloxycarbonyl)-3'-methoxycarbonyl)-2'-propenyl] prolinate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (2S)-cis-(Z)-1-(tert-butyloxycarbonyl)-5-[2'-(4-methoxy-phenyl)-(3'-amino-(N-benzyloxycarbonyl)-3'-methoxycarbonyl)-2'-propenyl] prolinate(478239-50-8)
EPA Substance Registry System: methyl (2S)-cis-(Z)-1-(tert-butyloxycarbonyl)-5-[2'-(4-methoxy-phenyl)-(3'-amino-(N-benzyloxycarbonyl)-3'-methoxycarbonyl)-2'-propenyl] prolinate(478239-50-8)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 478239-50-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 478239-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,2,3 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 478239-50:
(8*4)+(7*7)+(6*8)+(5*2)+(4*3)+(3*9)+(2*5)+(1*0)=188
188 % 10 = 8
So 478239-50-8 is a valid CAS Registry Number.

478239-50-8Upstream product

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478239-50-8Relevant academic research and scientific papers

Stereoselective bromination-suzuki cross-coupling of dehydroamino acids to form novel reverse-turn peptidomimetics: substituted unsaturated and saturated indolizidinone amino acids.

Zhang, Junyi,Xiong, Chiyi,Wang, Wei,Ying, Jinfa,Hruby, Victor J

, p. 4029 - 4032 (2007/10/03)

A general and efficient methodology has been developed to prepare the C4-substituted dipeptide reverse-turn mimetics unsaturated (9a, 10a) and saturated (11a) azabicyclo[4.3.0] alkane amino acid derivatives. The side chain was introduced by bromination of

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