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4-IODO-2,3-DIHYDRO-1H-INDOLE is a synthetic chemical compound belonging to the indole family, which are aromatic heterocyclic organic compounds. It features a bicyclic indole structure with an iodine atom attached to the four-position and a saturated bond between the twoand three-positions, hence the term "dihydro." Although scientific literature on this specific compound is limited, indoles are known for their versatile bioactivity and significance in medicinal chemistry.

939759-03-2

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939759-03-2 Usage

Uses

Used in Pharmaceutical Industry:
4-IODO-2,3-DIHYDRO-1H-INDOLE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its versatile bioactivity and structural features make it a valuable component in the development of new drugs.
Used in Medicinal Chemistry Research:
4-IODO-2,3-DIHYDRO-1H-INDOLE serves as a key compound in medicinal chemistry research, where it is studied for its potential applications in drug discovery and design. Its indole structure and iodine atom may contribute to unique interactions with biological targets, offering opportunities for the creation of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 939759-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,9,7,5 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 939759-03:
(8*9)+(7*3)+(6*9)+(5*7)+(4*5)+(3*9)+(2*0)+(1*3)=232
232 % 10 = 2
So 939759-03-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8IN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-3,10H,4-5H2

939759-03-2SDS

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 4-Iodoindoline

1.2 Other means of identification

Product number -
Other names 4-iodo-2,3-dihydro-1H-indole

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:939759-03-2 SDS

939759-03-2Downstream Products

939759-03-2Relevant academic research and scientific papers

Synthetic studies toward penitrem E: Enantiocontrolled construction of B-E rings

Yoshii, Yu,Otsu, Takanori,Hosokawa, Norihiko,Takasu, Kiyosei,Okano, Kentaro,Tokuyama, Hidetoshi

, p. 1070 - 1073 (2015)

Enantiocontrolled construction of B-E rings of penitrem E was accomplished from 4-iodoindole in 13 steps with an overall yield of 1.7%. Diastereoselective Tf2NH-catalyzed (2+2)-cycloaddition between silyl enol ether and methyl acrylate furnishe

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