Cas 87829-75-2,(R)-6-[((S)-5-Benzyloxycarbonyl-5-benzyloxycarbonylamino-pentylamino)-methyl]-2-(4-nitro-phenyl)-[1,3]oxazinane-3-carboxylic acid benzyl ester

87829-75-2

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Basic information

Product Name: (R)-6-[((S)-5-Benzyloxycarbonyl-5-benzyloxycarbonylamino-pentylamino)-methyl]-2-(4-nitro-phenyl)-[1,3]oxazinane-3-carboxylic acid benzyl ester
Synonyms:
CAS NO:87829-75-2
Molecular Formula:
Molecular Weight: 724.811
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: (R)-6-[((S)-5-Benzyloxycarbonyl-5-benzyloxycarbonylamino-pentylamino)-methyl]-2-(4-nitro-phenyl)-[1,3]oxazinane-3-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-6-[((S)-5-Benzyloxycarbonyl-5-benzyloxycarbonylamino-pentylamino)-methyl]-2-(4-nitro-phenyl)-[1,3]oxazinane-3-carboxylic acid benzyl ester(87829-75-2)
EPA Substance Registry System: (R)-6-[((S)-5-Benzyloxycarbonyl-5-benzyloxycarbonylamino-pentylamino)-methyl]-2-(4-nitro-phenyl)-[1,3]oxazinane-3-carboxylic acid benzyl ester(87829-75-2)

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: 87829-75-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87829-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,2 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87829-75:
(7*8)+(6*7)+(5*8)+(4*2)+(3*9)+(2*7)+(1*5)=192
192 % 10 = 2
So 87829-75-2 is a valid CAS Registry Number.

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87829-75-2Relevant academic research and scientific papers

Chemistry of Naturally Occurring Polyamines. 7. Selective Functionalization of Hydroxyputrescine

Tice, Colin M.,Ganem, Bruce

, p. 5043 - 5048 (2007/10/02)

As part of a program to synthesize biologically interesting polyamines and their conjugates, we report studies on the structure and reactivity of hydroxyputrescine-aldehyde adducts which permit regioselective functionalization of this rather rare naturall

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