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2,3-Dimethyl-6-iodo-2H-indeno[2,1-b]thiophene, a halogenated heterocyclic compound with the molecular formula C15H13IS, is characterized by the presence of both sulfur and iodine atoms in its structure. It is known for its high reactivity and ability to undergo various chemical reactions, making it a valuable building block in the field of organic chemistry. Its unique structure and properties also make it a potential candidate for the development of new molecules with diverse biological activities.

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  • 1234616-58-0 Structure
  • Basic information

    1. Product Name: 2,3-DiMethyl-6-iodo-2H-in...
    2. Synonyms: 2,3-DiMethyl-6-iodo-2H-in...;6-iodo-2,3-dimethyl-2H-indazole;C-8242
    3. CAS NO:1234616-58-0
    4. Molecular Formula: C9H9IN2
    5. Molecular Weight: 272.09
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1234616-58-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,3-DiMethyl-6-iodo-2H-in...(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-DiMethyl-6-iodo-2H-in...(1234616-58-0)
    11. EPA Substance Registry System: 2,3-DiMethyl-6-iodo-2H-in...(1234616-58-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1234616-58-0(Hazardous Substances Data)

1234616-58-0 Usage

Uses

Used in Organic Synthesis:
2,3-Dimethyl-6-iodo-2H-indeno[2,1-b]thiophene is used as a starting material in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and organic materials. Its high reactivity and ability to undergo various chemical reactions make it a valuable building block in this field.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-Dimethyl-6-iodo-2H-indeno[2,1-b]thiophene is used as a key intermediate for the synthesis of new molecules with potential therapeutic applications. Its unique structure and properties contribute to the development of innovative drugs with diverse biological activities.
Used in Agrochemical Industry:
2,3-Dimethyl-6-iodo-2H-indeno[2,1-b]thiophene is also utilized in the agrochemical industry as a precursor for the synthesis of new agrochemicals, such as pesticides and herbicides. Its reactivity and structural features enable the creation of novel compounds with improved efficacy and selectivity in agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1234616-58-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,6,1 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1234616-58:
(9*1)+(8*2)+(7*3)+(6*4)+(5*6)+(4*1)+(3*6)+(2*5)+(1*8)=140
140 % 10 = 0
So 1234616-58-0 is a valid CAS Registry Number.

1234616-58-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-iodo-2,3-dimethylindazole

1.2 Other means of identification

Product number -
Other names C-8242

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:1234616-58-0 SDS

1234616-58-0Downstream Products

1234616-58-0Relevant articles and documents

Regioselective methylation of indazoles using methyl 2,2,2- trichloromethylacetimidate

Baddam, Sudhakar Reddy,Uday Kumar,Panasa Reddy,Bandichhor, Rakeshwar

supporting information, p. 1661 - 1663 (2013/03/29)

An efficient and regio selective synthesis of substituted 2-methyl-2H-indazoles using a methyl 2,2,2-trichloroacetimidate is described.

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