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5349-29-1

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5349-29-1 Usage

General Description

2-Iodopropane-1,3-diol is a chemical compound with the molecular formula C3H7IO2. It is also known as 2-Iodo-1,3-propanediol and is classified as a halogenated alcohol. It is a colorless, viscous liquid that is used as a reagent in organic synthesis, particularly in the production of pharmaceuticals and other fine chemicals. The presence of the iodine atom in the molecule makes it useful for various reactions such as nucleophilic substitution and organometallic reactions. It is also known for its use as a building block in the synthesis of various organic compounds and is an important intermediate in the production of specialty chemicals. Additionally, it is used as a solvent and as a stabilizer in some biochemical reactions. Overall, 2-Iodopropane-1,3-diol has several important applications in organic synthesis and chemical manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 5349-29-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5349-29:
(6*5)+(5*3)+(4*4)+(3*9)+(2*2)+(1*9)=101
101 % 10 = 1
So 5349-29-1 is a valid CAS Registry Number.

5349-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodopropane-1,3-diol

1.2 Other means of identification

Product number -
Other names 2-iodo-propane-1,3-diol

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:5349-29-1 SDS

5349-29-1Relevant articles and documents

Structure-activity relationship of lipopeptide from outer membrane of Escherichia coli and synthesis of highly immunopotenting lipopeptide derivatives with an achiral lipo-part

Kurimura,Achiwa

, p. 627 - 629 (2007/10/02)

For outstanding the structure-activity relationship of lipopeptide derivatives, high biologically active lipopeptide derivatives with an achiral lipo-part were newly synthesized.

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