59956-66-0 Usage
General Description
3-Phenylpropyl bromoacetate is an organic chemical compound with the molecular formula C11H13BrO2. It is a colorless liquid with a sweet, fruit-like odor, and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 3-Phenylpropyl bromoacetate is an ester where the phenyl group is bonded to a 3-carbon propyl chain, which in turn is attached to a bromo group and an acetate group. It is flammable and may cause skin and eye irritation upon contact. 3-phenylpropyl bromoacetate is also known by the synonym Bromoacetic acid 3-phenylpropyl ester and is mainly used in laboratories and chemical manufacturing industries for various organic synthesis processes.
Check Digit Verification of cas no
The CAS Registry Mumber 59956-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,5 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59956-66:
(7*5)+(6*9)+(5*9)+(4*5)+(3*6)+(2*6)+(1*6)=190
190 % 10 = 0
So 59956-66-0 is a valid CAS Registry Number.
59956-66-0Relevant articles and documents
Synthesis of Elongated Esters from Alkenes
Miura, Tomoya,Funakoshi, Yuuta,Nakahashi, Junki,Moriyama, Daisuke,Murakami, Masahiro
supporting information, p. 15455 - 15459 (2018/10/31)
A convenient method for synthesizing elongated aliphatic esters from alkenes is reported. An (alkoxycarbonyl)methyl radical species is generated upon visible-light irradiation of an ester-stabilized phosphorus ylide in the presence of a photoredox catalyst. This radical species adds onto the carbon–carbon double bond of an alkene to produce an elongated aliphatic ester.
N,N′-ditosylhydrazine: A convenient reagent for facile synthesis of diazoacetates
Torna, Tatsuya,Shimokawa, Jun,Fukuyama, Tohru
, p. 3195 - 3197 (2008/02/10)
A novel entry to the synthesis of diazoacetates is disclosed. A variety of diazoacetates were synthesized from the corresponding bromoacetates by treatment with N,N′-ditosylhydrazine in moderate to high yields. Ease of operation with the stable crystalline reagent as well as a short reaction time offer a useful alternative to the conventional methods.
