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1577-30-6

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1577-30-6 Usage

Type of compound

Halogenated ketone

Bromine atoms

Contains two bromine atoms

Carbonyl group

Contains a carbonyl group

Usage

Commonly used as a reagent in organic synthesis

Application

Particularly in the production of pharmaceuticals and other fine chemicals

Physical state

Colorless liquid

Odor

Pungent

Reactivity

Highly reactive due to the presence of bromine atoms

Safety precautions

Potential irritant to the skin, eyes, and respiratory system

Handling

Should be handled with caution in a well-ventilated area with appropriate protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 1577-30-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1577-30:
(6*1)+(5*5)+(4*7)+(3*7)+(2*3)+(1*0)=86
86 % 10 = 6
So 1577-30-6 is a valid CAS Registry Number.

1577-30-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dibromoheptan-2-one

1.2 Other means of identification

Product number -
Other names 1,3-Dibromo-2-heptanone

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:1577-30-6 SDS

1577-30-6Upstream product

1577-30-6Downstream Products

1577-30-6Relevant articles and documents

Variation in the regioselectivity of levulinic acid bromination in ionic liquids

Zavozin, Alexander G.,Kravchenko, Natalya E.,Ignat'ev, Nikolay V.,Zlotin, Sergei G.

scheme or table, p. 545 - 547 (2010/10/02)

The reaction of levulinic acid and its esters with bromine in ionic liquids results in the formation of 3-bromo derivatives as the major products and not the 5-bromo substituted isomers, which are typically formed in organic solvents. The bromination of l

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