1577-29-3 Usage
Category
Organic compound
Subcategory
1,3-dibromopropanes
Physical State
Colorless to light yellow liquid
Odor
Pungent
Primary Use
Intermediate in the synthesis of pharmaceuticals and other organic compounds
Reactivity
Highly reactive
Flammability
Flammable
Safety Precaution
Should be handled with care
Additional Use
Reagent for the preparation of various organic compounds
Common Application
Research and laboratory settings
Chemical Structure
1,3-dibromo-4-methyl-2-pentanone backbone with a ketone functional group and a methyl substituent
Check Digit Verification of cas no
The CAS Registry Mumber 1577-29-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1577-29:
(6*1)+(5*5)+(4*7)+(3*7)+(2*2)+(1*9)=93
93 % 10 = 3
So 1577-29-3 is a valid CAS Registry Number.
1577-29-3Relevant articles and documents
Synthesis of the tricyclic core of vinigrol via an intramolecular diels-alder reaction
Grise, Christiane M.,Tessier, Guillaume,Barriault, Louis
, p. 1545 - 1548 (2008/02/02)
Equation presented Herein, we present a successful synthesis of the tricyclic core of vinigrol (1). Our approach takes advantage of a highly regioselective intramolecular Diels-Alder reaction of the diene 11 to construct two rings of the tricyclic vinigro
Formation of α-iminoketones and α-diimines versus Favorskii rearrangement products from the reaction of α,α′-dibromoketones and primary amines
De Kimpe, Norbert,D'Hondt, Luc,Mones, Luc
, p. 3183 - 3208 (2007/10/02)
The reaction of aliphatic acyclic α,α'-dibromoketones with primary amines gave rise to α-iminoketones and α-diimines. Both reaction products could be selectively obtained under appropriate reaction conditions. Sterically hindered α,α-dibromoketones did no