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Benzene, 1,4-bis[2-(4-bromo-2,5-dimethylphenyl)ethenyl]-2-iodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88111-68-6

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88111-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88111-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,1 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88111-68:
(7*8)+(6*8)+(5*1)+(4*1)+(3*1)+(2*6)+(1*8)=136
136 % 10 = 6
So 88111-68-6 is a valid CAS Registry Number.

88111-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-[2-[4-[2-(4-bromo-2,5-dimethylphenyl)ethenyl]-2-iodophenyl]ethenyl]-2,5-dimethylbenzene

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:88111-68-6 SDS

88111-68-6Downstream Products

88111-68-6Relevant academic research and scientific papers

Synthesis and Chiral Recognition of Novel Crown Ethers incorporating Helicene Chiral Centres

Nakazaki, Masao,Yamamoto, Koji,Ikeda, Tetsumi,Kitsuki, Tomohito,Okamoto, Yoshio

, p. 787 - 788 (1983)

Two novel optically active crown ethers (7) and (14) incorporating helicene molecular frameworks were prepared, and their chiral recognition properties were examined to show that (M)-(-)-(7) and (M)-(-)-(14) had opposite chiral recognition for the transpo

Synthesis and Chiral Recognition of Optically Active Crown Ethers incorporating a Helicene Moiety as the Chiral Centre

Yamamoto, Koji,Ikeda, Tetsuo,Kitsuki, Tomihito,Okamoto, Yoshio,Chikamatsu, Hiroaki,Nakazaki, Masao

, p. 271 - 276 (2007/10/02)

The synthesis of optically active crown ethers (8), (14), and (18) incorporating helicene molecular frameworks is reported.Their chiral recognition properties have been examined and show that (M)-(-)-(14), although of the same helicity as (M)-(-)-(8) and

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