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5094-41-7

2,3-DiMethyl-1H-indole-7-carbohydrazide, also known as DMICH, is a chemical compound with the molecular formula C12H14N4O. It is a derivative of indole and carbohydrazide, characterized by its unique structure and properties. DMICH serves as a versatile building block in organic synthesis and pharmaceutical research, making it a promising candidate for the development of various chemical compounds.

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  • 5094-41-7 Structure

  • Basic information

    1. Product Name: 2,3-DiMethyl-1H-indole-7-carbohydrazide
    2. Synonyms: 2,3-DiMethyl-1H-indole-7-carbohydrazide
    3. CAS NO:5094-41-7
    4. Molecular Formula:
    5. Molecular Weight: 203.24042
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5094-41-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    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-1H-indole-7-carbohydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-DiMethyl-1H-indole-7-carbohydrazide(5094-41-7)
    11. EPA Substance Registry System: 2,3-DiMethyl-1H-indole-7-carbohydrazide(5094-41-7)

  • 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: 5094-41-7(Hazardous Substances Data)

5094-41-7 Usage

Uses

Used in Pharmaceutical Research:
2,3-DiMethyl-1H-indole-7-carbohydrazide is used as a key intermediate in the synthesis of anti-tumor and antimicrobial agents. Its unique structure allows for the development of novel compounds with potential therapeutic applications, contributing to the advancement of medicinal chemistry.
Used in Organic Synthesis:
DMICH is utilized as a versatile building block in the creation of diverse chemical compounds. Its properties make it suitable for various organic synthesis processes, enabling the production of a wide range of compounds with different applications.
Used in the Synthesis of Novel Heterocyclic Compounds:
2,3-DiMethyl-1H-indole-7-carbohydrazide is employed as a starting material in the synthesis of novel heterocyclic compounds. Its unique structure and reactivity facilitate the formation of new heterocyclic systems, expanding the scope of chemical compounds available for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5094-41-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,9 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5094-41:
(6*5)+(5*0)+(4*9)+(3*4)+(2*4)+(1*1)=87
87 % 10 = 7
So 5094-41-7 is a valid CAS Registry Number.

5094-41-7SDS

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 2,3-dimethyl-indole-7-carboxylic acid hydrazide

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-indol-7-carbonsaeure-hydrazid

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:5094-41-7 SDS

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