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Propanedioic acid, bromo-, bis[(1S)-1-phenylbutyl] ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

173202-60-3

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173202-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173202-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,2,0 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 173202-60:
(8*1)+(7*7)+(6*3)+(5*2)+(4*0)+(3*2)+(2*6)+(1*0)=103
103 % 10 = 3
So 173202-60-3 is a valid CAS Registry Number.

173202-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[(1S)-1-phenylbutyl] 2-bromopropanedioate

1.2 Other means of identification

Product number -
Other names -

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:173202-60-3 SDS

173202-60-3Upstream product

173202-60-3Downstream Products

173202-60-3Relevant academic research and scientific papers

Multiple Cyclopropanations of C70. Synthesis and Characterization of Bis-, Tris-, and Tetrakis-adducts and Chiroptical Properties of Bis-adducts with Chiral Addends, Including a Recommendation for the Configurational Description of Fullerene Derivatives w

Herrmann, Andreas,Ruettimann, Markus,Thilgen, Carlo,Diederich, Francois

, p. 1673 - 1704 (2007/10/02)

The regioselectivity of multiple cyclopropanations of C70 with 2-bromopropanedioates in the presence of 1,8-diazabicycloundec-7-ene (DBU) as base (Bingel reaction) was investigated in a systematic study.Bis-adduct formation occurred preferentially

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