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4-(2-bromophenyl)-2-methyl-2-butanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183864-47-3

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183864-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183864-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,8,6 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 183864-47:
(8*1)+(7*8)+(6*3)+(5*8)+(4*6)+(3*4)+(2*4)+(1*7)=173
173 % 10 = 3
So 183864-47-3 is a valid CAS Registry Number.

183864-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-bromophenyl)-2-methyl-2-butanol

1.2 Other means of identification

Product number -
Other names 2-Bromo-α,α-dimethylbenzenepropanol

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:183864-47-3 SDS

183864-47-3Upstream product

183864-47-3Relevant academic research and scientific papers

Catalyst for aromatic C—O, C—N, and C—C bond formation

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, (2008/06/13)

The present invention is directed to a transition metal catalyst, comprising a Group 8 metal and a ligand having the structure wherein R, R′ and R″ are organic groups having 1-15 carbon atoms, n=1-5, and m=0-4. The present invention is also directed to a method of forming a compound having an aromatic or vinylic carbon-oxygen, carbon-nitrogen, or carbon-carbon bond using the above catalyst. The catalyst and the method of using the catalyst are advantageous in preparation of compounds under mild conditions of approximately room temperature and pressure.

Gem-dialkyl-7-oxabicycloheptyl substituted heterocyclic amide prostaglandin analogs useful in the treatment of thrombotic and vasospastic disease

-

, (2008/06/13)

Gem-dialkyl-7-oxabicycloheptane substituted prostaglandin analogs useful in treating thrombotic and vasospastic disease have the structural formula wherein m is 1, 2 or 3; n is 0, 1, 2, 3 or 4;, Z is -(CH2)2-, -CH=CH- or with the proviso when Z is -CH=CH-, n is l, 2, 3 or 4; R is CO2H, CO2lower alkyl, or CO2alkali metal, X is O or NH; and where R1 and R2 are as defined herein and R3 and R4 are each independently alkyl, or R3 and R4 may be taken together with the carbon to which it is attached to form a 3- or 4-membered ring.

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