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5-bromo-6-(2,3-dibromopropyl)-1,3-benzodioxole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56312-11-9

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56312-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56312-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,1 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56312-11:
(7*5)+(6*6)+(5*3)+(4*1)+(3*2)+(2*1)+(1*1)=99
99 % 10 = 9
So 56312-11-9 is a valid CAS Registry Number.

56312-11-9SDS

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 5-bromo-6-(2,3-dibromopropyl)-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names 5-bromo-6-(2,3-dibromo-propyl)-benzo[1,3]dioxole

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:56312-11-9 SDS

56312-11-9Downstream Products

56312-11-9Relevant academic research and scientific papers

Reaction of Aromatic and Unsaturated Compounds with the Potassium Permanganate/HCI (HBr) Acetonitrile Reagent

Liu, Lilian Kao,Lin, Ching-Shan

, p. 61 - 66 (2007/10/03)

Addition of hydrochloric or hydrobromic acid to a solution of potassium permanganate in acetonitrile produced a homogeneous mixture, which is suitable for laboratory chlorination or bromination, respectively. Aromatic compounds more reactive than alkylbenzenes can be chlorinated or brominated without additional catalyst. Alkenes and alkynes give the corresponding vicinal dihaloalkanes and vinyl halides. All reactions complete within two hours under mild condition (25-60 °C) with excellent to moderate yields.

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