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5365-17-3

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5365-17-3 Usage

Appearance

Colorless to pale yellow liquid The compound's physical state and color at room temperature.

Odor

Strong bromine The compound has a noticeable and pungent bromine smell.

Usage

Intermediate in pharmaceuticals and agrochemicals It is mainly used as an intermediate compound in the synthesis of various pharmaceuticals and agrochemicals.

Usage

Organic synthesis The compound is also used in organic synthesis for creating other organic compounds.

Usage

Building block in complex organic compounds It serves as a building block for the preparation of more complex organic compounds.

Reactivity

Highly reactive The compound is known for its high reactivity, which necessitates careful handling.

Hazards

Corrosive The compound has corrosive properties, which can cause damage to materials and surfaces it comes into contact with.

Hazards

Toxic The compound is toxic, and exposure can pose health risks. It should be handled with care to avoid harm.

Check Digit Verification of cas no

The CAS Registry Mumber 5365-17-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5365-17:
(6*5)+(5*3)+(4*6)+(3*5)+(2*1)+(1*7)=93
93 % 10 = 3
So 5365-17-3 is a valid CAS Registry Number.

5365-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dibromocyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,2-dibromocyclopropanecarboxylic acid

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:5365-17-3 SDS

5365-17-3Relevant articles and documents

Thermodynamic control of diastereoselectivity in the formal nucleophilic substitution of bromocyclopropanes

Banning, Joseph E.,Prosser, Anthony R.,Rubin, Michael

, p. 1488 - 1491 (2010)

(Figure Presented) A new, general, and chemoselective protocol for the formal nucleophilic substitution of 2-bromocyclopropylcarboxamides is described. A wide range of alcohols and phenols can be employed as pronucleophiles in this transformation, providi

Highly diastereoselective formal nucleophilic substitution of bromocyclopropanes

Alnasleh, Bassam K.,Sherrill, William M.,Rubina, Marina,Banning, Joseph,Rubin, Michael

supporting information; experimental part, p. 6906 - 6907 (2009/09/26)

-

6-(Substituted-cycloalkylcarboxamide) penicillanic acids

-

, (2008/06/13)

Penicillins of the formula SPC1 Or a pharmaceutically-acceptable, nontoxic salt thereof, Wherein R1 and R2 are the same or different and each is hydrogen, fluorine, chlorine or bromine; or when R2 is hydrogen, R1 can also be cyano, hydroxyl, azido, amino or nitro; or R1 and R2 are bonded to a ring carbon atom and constitute a single oxygen atom; R3 is hydrogen, methyl, chlorine, bromine, cyano, methoxy or carboxyl; and n is 2 to 7; Are useful for their antibacterial activity.

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