Cas 918134-14-2,1-Pyrrolidinecarboxylic acid, 2-[[[(4-nitrophenyl)sulfonyl]amino]methyl]-, 1,1-dimethylethyl ester, (2S)-

918134-14-2

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Basic information

Product Name: 1-Pyrrolidinecarboxylic acid, 2-[[[(4-nitrophenyl)sulfonyl]amino]methyl]-, 1,1-dimethylethyl ester, (2S)-
Synonyms:
CAS NO:918134-14-2
Molecular Formula: C16H23N3O6S
Molecular Weight: 385.441
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: 1-Pyrrolidinecarboxylic acid, 2-[[[(4-nitrophenyl)sulfonyl]amino]methyl]-, 1,1-dimethylethyl ester, (2S)-(CAS DataBase Reference)
NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 2-[[[(4-nitrophenyl)sulfonyl]amino]methyl]-, 1,1-dimethylethyl ester, (2S)-(918134-14-2)
EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 2-[[[(4-nitrophenyl)sulfonyl]amino]methyl]-, 1,1-dimethylethyl ester, (2S)-(918134-14-2)

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: 918134-14-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 918134-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,1,3 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 918134-14:
(8*9)+(7*1)+(6*8)+(5*1)+(4*3)+(3*4)+(2*1)+(1*4)=162
162 % 10 = 2
So 918134-14-2 is a valid CAS Registry Number.

918134-14-2Upstream product

168049-26-1 tert-butyl (2S)-2-(azidomethyl)-1-pyrrolidinecarboxylate

918134-14-2Downstream Products

918134-14-2Relevant academic research and scientific papers

Synthesis and thermal reactivity of pyrrolidine- and 2-pyrrolidinone-fused cyclic enediynes

Roy, Basab,Basak, Amit

, p. 2804 - 2806 (2006)

Various bicyclic enediynes containing pyrrolidine and pyrrolidinone moieties were synthesised. Thermal reactivity studies indicated the lowering of the onset temperature for Bergman cyclisation upon fusion of these heterocyclic systems onto the cyclic ene

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