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Benzene, 1,1'-(4-bromo-1-butenylidene)bis[4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111448-46-5

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111448-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111448-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 111448-46:
(8*1)+(7*1)+(6*1)+(5*4)+(4*4)+(3*8)+(2*4)+(1*6)=95
95 % 10 = 5
So 111448-46-5 is a valid CAS Registry Number.

111448-46-5SDS

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 1-[4-bromo-1-(4-methoxyphenyl)but-1-enyl]-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names 4-bromo-1,1-bis(4-methoxyphenyl)but-1-ene

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:111448-46-5 SDS

111448-46-5Downstream Products

111448-46-5Relevant academic research and scientific papers

A method for synthesis of homoallylic bromide

Qi, Wenke,Wang, Peipei,Fan, Liyuan,Zhang, Songlin

, p. 5918 - 5924 (2013/07/26)

Cyclopropyl Grignard reagents react with carbonyl compounds in the presence of diethyl phosphite to give homoallylic bromides. The reaction is effectively carried out under mild conditions in a one-pot fashion with moderate to good yields.

Synthesis and SAR study of diphenylbutylpiperidines as cell autophagy inducers

Chen, Gang,Xia, Hongguang,Cai, Yu,Ma, Dawei,Yuan, Junying,Yuan, Chengye

scheme or table, p. 234 - 239 (2011/02/26)

A novel series of diphenylbutylpiperidines as autophagy inducers was described and extensive SAR studies resulted in derivatives (15d-e, 15i-j) with 10-fold greater activity than the lead compounds 1 and 2. Meanwhile, a new synthetic route to diphenylbutyl bromide (6) from bromobenzene and γ-butyrolactone was also reported here.

DIPHENYLBUTYPIPERIDINE AUTOPHAGY INDUCERS

-

Page/Page column 7; 84-85, (2011/12/02)

Autophagy inducing compounds, methods of their preparation and use, and kits containg said compounds are disclosed herein.

Ring-opening reaction of methylenecyclopropanes with LiCl, LiBr or NaI in acetic acid

Huang, Jin-Wen,Shi, Min

, p. 2057 - 2062 (2007/10/03)

The methylenecyclopropanes 1 react with LiCl, LiBr or NaI at 80°C to give the corresponding gem-disubstituted homoallylic halides 2 in good to excellent yields in acetic acid. In some cases, the ring-opening reaction can be completed within 5 min to give

Diarylalkyl-substituted alkylamines and medicaments containing them

-

, (2008/06/13)

A compound I STR1 in which R1 is cycloalkyl, alkenyl, cycloalkenyl, phenyl, STR2 where J, L, M, and E are methine or nitrogen and J', L', M', and E' are methylene, carbonyl or imino; R2 is phenyl or phenylalkyl; a is various amine ra

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