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108350-39-6

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108350-39-6 Usage

General Description

2-Iodo-1-phenyl-1-butanone is a chemical compound with the molecular formula C10H11IO. It is a pale yellow to brown liquid with a strong, sweet, and camphor-like odor. 2-Iodo-1-phenyl-1-butanone is used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is also used as a reagent in organic chemical reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Due to its chemical properties, 2-Iodo-1-phenyl-1-butanone should be handled and used with care, as it can be harmful if ingested, inhaled, or in contact with the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 108350-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,5 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108350-39:
(8*1)+(7*0)+(6*8)+(5*3)+(4*5)+(3*0)+(2*3)+(1*9)=106
106 % 10 = 6
So 108350-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11IO/c1-2-9(11)10(12)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3

108350-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodo-1-phenylbutan-1-one

1.2 Other means of identification

Product number -
Other names 2-IODO-1-PHENYL-1-BUTANONE

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:108350-39-6 SDS

108350-39-6Relevant articles and documents

Mercury(II) Chloride-Iodine: A Useful Reagent for the Direct and Regiospecific Synthesis of α-Iodocarbonyl Compounds

Barluenga, Jose,Martinez-Gallo, Jose M.,Najera, Carmen,Yus, Miguel

, p. 678 - 680 (1986)

α-Iodoaldehydes and α-iodoketones are obtained by direct iodination of the corresponding carbonyl compounds with mercury(II) chloride-iodine in a regiospecific manner.

Synthesis of α-heterosubstituted ketones through sulfur mediated difunctionalization of internal alkynes

Zhang, Zhong,Luo, Yuzheng,Du, Hongguang,Xu, Jiaxi,Li, Pingfan

, p. 5156 - 5161 (2019/06/05)

Synthesis of α-heterosubstituted ketones was achieved through sulfur mediated difunctionalization of internal alkynes in one pot. The reaction design involves: phenyl substituted internal alkyne attacking triflic anhydride activated diphenyl sulfoxide to

Direct metal-free α-iodination of arylketones induced by iodine or iodomethane with HTIB in ionic liquid

Lee, Jong Chan,Kim, Jimi,Park, Hyun Jung,Kwag, Byungmook,Lee, Seung Bae

experimental part, p. 1385 - 1386 (2010/09/18)

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