Cas 1260243-89-7,tert-butyl (S)-1-[(S)-3-benzyloxycarbonylamino-4-tert-butoxy-4-oxobutyl]-5-oxopyrrolidine-2-carboxylate

1260243-89-7

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Basic information

Product Name: tert-butyl (S)-1-[(S)-3-benzyloxycarbonylamino-4-tert-butoxy-4-oxobutyl]-5-oxopyrrolidine-2-carboxylate
Synonyms: tert-butyl (S)-1-[(S)-3-benzyloxycarbonylamino-4-tert-butoxy-4-oxobutyl]-5-oxopyrrolidine-2-carboxylate
CAS NO:1260243-89-7
Molecular Formula:
Molecular Weight: 476.57
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: tert-butyl (S)-1-[(S)-3-benzyloxycarbonylamino-4-tert-butoxy-4-oxobutyl]-5-oxopyrrolidine-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (S)-1-[(S)-3-benzyloxycarbonylamino-4-tert-butoxy-4-oxobutyl]-5-oxopyrrolidine-2-carboxylate(1260243-89-7)
EPA Substance Registry System: tert-butyl (S)-1-[(S)-3-benzyloxycarbonylamino-4-tert-butoxy-4-oxobutyl]-5-oxopyrrolidine-2-carboxylate(1260243-89-7)

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: 1260243-89-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260243-89-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,2,4 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1260243-89:
(9*1)+(8*2)+(7*6)+(6*0)+(5*2)+(4*4)+(3*3)+(2*8)+(1*9)=127
127 % 10 = 7
So 1260243-89-7 is a valid CAS Registry Number.

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1260243-89-7Relevant academic research and scientific papers

Efficient synthesis of nicotianamine and non-natural analogues

Bouazaoui, M'Barek,Larrouy, Manuel,Martinez, Jean,Cavelier, Florine

, p. 6609 - 6617 (2010)

An efficient synthesis of nicotianamine has been achieved by using a new strategy based on N-alkylation. Sulfonamide activation proved to be necessary for the alkylation of the primary amine and the 2-(trimethylsilyl)ethanesulfonyl group was easily introd

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