Cas 160252-83-5,1-acetoxy-3-<(4-azidophthalimido)ethyl>-4-bromomethyl-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrole

160252-83-5

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Basic information

Product Name: 1-acetoxy-3-<(4-azidophthalimido)ethyl>-4-bromomethyl-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrole
Synonyms: 1-acetoxy-3-<(4-azidophthalimido)ethyl>-4-bromomethyl-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrole
CAS NO:160252-83-5
Molecular Formula:
Molecular Weight: 490.357
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-acetoxy-3-<(4-azidophthalimido)ethyl>-4-bromomethyl-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrole(CAS DataBase Reference)
NIST Chemistry Reference: 1-acetoxy-3-<(4-azidophthalimido)ethyl>-4-bromomethyl-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrole(160252-83-5)
EPA Substance Registry System: 1-acetoxy-3-<(4-azidophthalimido)ethyl>-4-bromomethyl-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrole(160252-83-5)

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: 160252-83-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160252-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,5 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 160252-83:
(8*1)+(7*6)+(6*0)+(5*2)+(4*5)+(3*2)+(2*8)+(1*3)=105
105 % 10 = 5
So 160252-83-5 is a valid CAS Registry Number.

160252-83-5Upstream product

55738-75-5 (2,5-dihydro-2,2,5,5-tetramethyl-1-oxyl-1H-pyrrol-3-yl)methanol

160252-83-5Downstream Products

160252-83-5Relevant academic research and scientific papers

Crosslinking 2,5-dihydro-1H-pyrrol-1-yloxyl spin-label reagents bifunctionalized with azidophthalimidyl and methylthiosulfonyloxy groups

Kalai,Roznyai,Jerkovich,Hideg

, p. 1079 - 1082 (2007/10/02)

Oxy-Cope and ortho ester Claisen rearrangements of 5- and 6-membered N-oxyl radicals were carried out. The resulting more stable 5-membered bromo derivative 6 was used in the synthesis of bifunctionalized crosslinking photo- and thiol-label 12.

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