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Propanedioic acid, phenyl-, mono(1,1-dimethylethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55610-35-0

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55610-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55610-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,1 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55610-35:
(7*5)+(6*5)+(5*6)+(4*1)+(3*0)+(2*3)+(1*5)=110
110 % 10 = 0
So 55610-35-0 is a valid CAS Registry Number.

55610-35-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(2-methylpropan-2-yl)oxy]-3-oxo-2-phenylpropanoate

1.2 Other means of identification

Product number -
Other names tert-Butylhydrogenphenylmalonat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55610-35-0 SDS

55610-35-0Relevant academic research and scientific papers

Highly enantioselective synthesis of α,α-dialkylmalonates by phase-transfer catalytic desymmetrization

Hong, Suckchang,Lee, Jihye,Kim, Minsik,Park, Yohan,Park, Cheonhyoung,Kim, Mi-Hyun,Jew, Sang-Sup,Park, Hyeung-Geun

supporting information; experimental part, p. 4924 - 4929 (2011/06/10)

A novel enantioselective synthetic method for the construction of a quaternary carbon center from malonates via phase-transfer catalytic (PTC) alkylation has been developed. The asymmetric α-alkylation of diphenylmethyl tert-butyl α-alkylmalonates with alkylating agents under phase-transfer catalysis conditions (aq 50% KOH, toluene, 0°C) in the presence of (S,S)-3,4,5-trifluorophenyl-NAS bromide (8) as PTC catalyst afforded the corresponding α,α-dialkylmalonates in high chemical (up to 99%) and optical yields (up to 97% ee) which could be readily converted to versatile chiral intermediates. Notably, the direct double α-alkylations of diphenylmethyl tert-butyl malonate also provided the corresponding α,α-dialkylmalonates without loss of enantioselectivity. The synthetic potential of this method has been demonstrated by the preparation of α,α-dialkylamino acid and oxindole systems.

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