Cas 1161880-99-4,tert-butyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)-2-phenylethylcarbamate

1161880-99-4

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Basic information

Product Name: tert-butyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)-2-phenylethylcarbamate
Synonyms: tert-butyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)-2-phenylethylcarbamate
CAS NO:1161880-99-4
Molecular Formula:
Molecular Weight: 537.367
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-(2-bromo-3,5-dinitrophenethylcarbamoyl)-2-phenylethylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)-2-phenylethylcarbamate(1161880-99-4)
EPA Substance Registry System: tert-butyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)-2-phenylethylcarbamate(1161880-99-4)

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: 1161880-99-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1161880-99-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,1,8,8 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1161880-99:
(9*1)+(8*1)+(7*6)+(6*1)+(5*8)+(4*8)+(3*0)+(2*9)+(1*9)=164
164 % 10 = 4
So 1161880-99-4 is a valid CAS Registry Number.

1161880-99-4Upstream product

1161880-99-4Downstream Products

1161881-24-8 tert-butyl (S)-1-(5,7-dinitroindolin-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate

1161880-99-4Relevant academic research and scientific papers

Preparation of photoactivable amino acid derivatives

Debieux, Jean-Luc,Bochet, Christian G.

supporting information; experimental part, p. 4519 - 4524 (2009/10/17)

(Chemical Equation Presented) A range of N-protected-R-amino acyl-5,7-dinitroindolines 3a-z were prepared in good yields from commercially available N-protected-R-amino acids 1a-z by a two-step sequence of acylation and intramolecular amide N-arylation. S

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