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1,2-diiodopropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

598-29-8

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598-29-8 Usage

Physical state

Colorless liquid

Odor

Strong

Uses

a. Solvent in chemical synthesis
b. Reagent in chemical synthesis
c. Introducing iodine into organic molecules
d. Starting material in the production of pharmaceuticals and agrochemicals
e. Manufacturing of optical brighteners
f. Manufacturing of antifungals

Reactivity

Highly reactive due to the presence of two iodine atoms

Reaction type

Substitution reactions with nucleophiles

Hazard classification

Classified as a hazardous substance

Toxicity

Toxic

Irritation

Irritating properties

Handling precautions

Should be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 598-29-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 598-29:
(5*5)+(4*9)+(3*8)+(2*2)+(1*9)=98
98 % 10 = 8
So 598-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H6I2/c1-3(5)2-4/h3H,2H2,1H3

598-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diiodopropane

1.2 Other means of identification

Product number -
Other names Propane,1,2-diiodo-(7CI,8CI,9CI)

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:598-29-8 SDS

598-29-8Upstream product

598-29-8Relevant academic research and scientific papers

The Reaction of Propene with Iodine Bromide

Alberts, Vincent,Carman, Raymond M.

, p. 455 - 459 (2007/10/02)

Iodobromination of propene gives a mixture (c. 60:40) of 2-bromo-1-iodopropane and 1-bromo-2-iodopropane.This mixture of kinetic control converts into an equilibrium (c. 70:30) mixture with heat.The addition to the double bond is postulated to occur through a bridged iodonium ion rather than through a simple carbocation, and hence Markownikoff's rule need not apply to this system

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