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2-Dodecanol, 1-bromo- is an organic compound with the chemical formula C12H25BrO. It is a colorless liquid at room temperature and has a molecular weight of 249.24 g/mol. 2-Dodecanol, 1-bromo- is a derivative of 2-dodecanol, where a bromine atom is attached to the first carbon atom of the dodecyl chain. It is used as a chemical intermediate in the synthesis of various organic compounds, such as surfactants, pharmaceuticals, and agrochemicals. Due to its reactivity, it is essential to handle 2-dodecanol, 1-bromo- with proper safety measures, including the use of gloves, goggles, and a well-ventilated workspace.

4107-57-7

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4107-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4107-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4107-57:
(6*4)+(5*1)+(4*0)+(3*7)+(2*5)+(1*7)=67
67 % 10 = 7
So 4107-57-7 is a valid CAS Registry Number.

4107-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromododecan-2-ol

1.2 Other means of identification

Product number -
Other names 2-Dodecanol,1-bromo

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:4107-57-7 SDS

4107-57-7Upstream product

4107-57-7Relevant academic research and scientific papers

Regio-and stereoselective hydroxybromination and dibromination of olefins using ammonium bromide and oxone

MacHarla, Arun Kumar,Chozhiyath Nappunni, Rohitha,Nama, Narender

supporting information; experimental part, p. 1401 - 1405 (2012/04/04)

An efficient protocol for the synthesis of vicinal bromohydrins and dibromides from olefins is presented. Various olefins are regio-and stereoselectively hydroxybrominated and dibrominated with anti fashion, following Markonikov's rule, using eco-friendly, non-toxic, and stable reagents such as NH4Br and oxone in CH3CN/H2O (1:1) and CH3CN without employing catalyst in moderate to excellent yields. Bromohydrins are formed instantaneously.

Facile one-pot synthesis of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent

Patil, Rajendra D.,Joshi, Girdhar,Adimurthy, Subbarayappa,Ranu, Brindaban C.

experimental part, p. 2529 - 2532 (2009/09/06)

A new method for the preparation of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent has been developed. Several α-bromoketones were successfully prepared from a variety of olefins by this method. This procedure is an alternative to conventional molecular bromine.

Micellar Effects upon Alkene Bromination. 2. The Role of Alkene Hydrophobicity

Cerichelli, Giorgio,Grande, Celeste,Luchetti, Luciana,Mancini, Giovanna

, p. 3025 - 3030 (2007/10/02)

Surface polarity of cettyltrimethylammonium bromide (CTAB) aqueous micelles was checked by use of as a probe the bromination reaction of a series of 1-alkenes and a water-soluble alkene, cis-4-cyclohexene-1,2-dicarboxylic acid dimethyl ester (I).There was

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