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1-Bromo-2-chloropropane, also known as 2-chloro-1-bromopropane or 1,2-dibromopropane, is a halogenated alkane with the chemical formula C3H6BrCl. It is a colorless liquid with a pungent odor and is used as a solvent, intermediate in the synthesis of various organic compounds, and in the production of pharmaceuticals. Due to its high reactivity and potential health risks, it is classified as a hazardous substance and requires proper handling and storage.

3017-96-7

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3017-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3017-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3017-96:
(6*3)+(5*0)+(4*1)+(3*7)+(2*9)+(1*6)=67
67 % 10 = 7
So 3017-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H6BrCl/c1-3(5)2-4/h3H,2H2,1H3

3017-96-7SDS

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-BROMO-2-CHLOROPROPANE

1.2 Other means of identification

Product number -
Other names 2-Chlor-1-brom-propan

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:3017-96-7 SDS

3017-96-7Downstream Products

3017-96-7Relevant academic research and scientific papers

BiX3 as an efficient and selective reagent for the halogen exchange reaction

Boyer, Bernard,Keramane, El Mehdi,Arpin, Severine,Montero, Jean-Louis,Roque, Jean-Pierre

, p. 1971 - 1976 (2007/10/03)

Bismuth halides are efficient and selective reagents in the halogen exchange reactions carried out under mild conditions. This rapid, high yield reaction proceeds mainly with retention of configuration.

COMPETITION BETWEEN n,?- AND n,?-ORBITAL INTERACTIONS IN CHLORINATED ETHERS R-O-CHClR1

Bredikhin, A. A.,Kirillovich, V. A.,Safin, I. A.,Vereshchagin, A. N.

, p. 2185 - 2189 (2007/10/02)

Using the AM-1 method, we have studied CH2=CH-O-CHClR1 molecules (R1 = H, Me).We have shown that the sc conformation with respect to the Csp3-O bond is preferred.We have systematized the 35Cl NOR data on the degree of manifestation of the generalized anomeric effect in R-OCHClR1 2C(=O)> molecules.We have established that enhancement of n,? conjugation in the R-O fragment leads to weakening of the n,? interaction in the O-C-Cl triad.

Efficient Conversion of Alkyl Chlorides into Bromides

Yoon, K. B.,Kochi, J. K.

, p. 1013 - 1014 (2007/10/02)

The convenient and selective catalytic conversion of secondary and tertiary alkyl chlorides into bromides with hydrogen bromide in the presence of small amounts of anhydrous iron(III) bromide is described.

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