Cas 121702-32-7,(2R,9S)-9-Benzyloxycarbonylamino-5,10-dioxo-[1,6]diazecane-2-carboxylic acid tert-butyl ester

121702-32-7

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Basic information

Product Name: (2R,9S)-9-Benzyloxycarbonylamino-5,10-dioxo-[1,6]diazecane-2-carboxylic acid tert-butyl ester
Synonyms:
CAS NO:121702-32-7
Molecular Formula:
Molecular Weight: 419.478
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: (2R,9S)-9-Benzyloxycarbonylamino-5,10-dioxo-[1,6]diazecane-2-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,9S)-9-Benzyloxycarbonylamino-5,10-dioxo-[1,6]diazecane-2-carboxylic acid tert-butyl ester(121702-32-7)
EPA Substance Registry System: (2R,9S)-9-Benzyloxycarbonylamino-5,10-dioxo-[1,6]diazecane-2-carboxylic acid tert-butyl ester(121702-32-7)

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: 121702-32-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121702-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,0 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121702-32:
(8*1)+(7*2)+(6*1)+(5*7)+(4*0)+(3*2)+(2*3)+(1*2)=77
77 % 10 = 7
So 121702-32-7 is a valid CAS Registry Number.

121702-32-7Upstream product

121673-21-0 (R)-1-((S)-2-Benzyloxycarbonylamino-4-carbamoyl-butyryl)-5-oxo-pyrrolidine-2-carboxylic acid tert-butyl ester

121702-32-7Downstream Products

121702-32-7Relevant academic research and scientific papers

A CONVENIENT PREPARATION OF DERIVATIVES OF 3(S)-AMINO-10(R)-CARBOXY-1,6-DIAZA-CYCLODECA-2,7-DIONE THE DILACTAM OF L-α,γ-DIAMINOBUTYRIC ACID AND D-GLUTAMIC ACID: A β-TURN TEMPLATE

Kemp, D.S.,Stites, Wesley E.

, p. 5057 - 5060 (2007/10/02)

The title compound has been prepared as its N-benzylcarbonyl urethane in a three-step one-pot reaction in 20-30percent yield from the dipeptide derivative Z-Gln-Glu(OH)2.Evidence concerning the configuration and chiral purity of the title compound is given.

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