62248-40-2 Usage
General Description
2,3-dibromo-3-phenylpropanal is a chemical compound with the molecular formula C9H8Br2O. It is a colorless to pale yellow liquid that is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. 2,3-dibromo-3-phenylpropanal is also known for its ability to act as a reactant in the formation of various organic compounds. It is regarded as a versatile chemical that can undergo a variety of reactions, including nucleophilic addition reactions, which makes it useful in organic synthesis. Additionally, this compound is known for its ability to act as a reagent in organic reactions, particularly in the functionalization of aromatic compounds. Overall, 2,3-dibromo-3-phenylpropanal is a key component in the synthesis of various organic compounds and plays a vital role in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 62248-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62248-40:
(7*6)+(6*2)+(5*2)+(4*4)+(3*8)+(2*4)+(1*0)=112
112 % 10 = 2
So 62248-40-2 is a valid CAS Registry Number.
62248-40-2Relevant articles and documents
A convenient halogenation of α,β-unsaturated carbonyl compounds with OXONE and hydrohalic acid (HBr,HCl)
Kim, Kyoung-Mahn,Park, In-Hwan
, p. 2641 - 2644 (2007/10/03)
Mixtures of OXONE and hydrobromic acid or hydrochloric acid afford solutions of bromine or chlorine, respectively, α-Bromo- or α-chloro-α,β-unsaturated carbonyl compounds were prepared by addition of hydrobromic acid or hydrochloric acid to the mixture of
Selective regeneration of carbonyl compounds from oximes with N-bromosuccinimide under neutral and mild conditions
Bandgar, Babasaheb P.,Kale, Ramesh R.,Kunde, Lalita B.
, p. 1057 - 1060 (2007/10/03)
N-Bromosuccinimide has been found to be an efficient and selective reagent for the mild oxidative cleavage of oximes to yield their corresponding carbonyl compounds in good to excellent yields.
α-Keto Dianion Precursors via Conjugate Additions to Cyclic α-Bromo Enones
Kowalski, Conrad J.,Weber, Ann E.,Fields, Kevin W.
, p. 5088 - 5093 (2007/10/02)
Successful conjugate to 2-bromocyclohexenone and 2-bromocyclopentenone have been achieved with a variety of lithium homocuprates, mixed cyanocuprates, and lithium tri-sec-butylborohydride as well.In all cases the resulting α-bromo enolate anions could be
