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Methyl 5-amino-1H-imidazole-4-carboxylate hydrochloride is a chemical compound with the molecular formula C6H8N4O2HCl. It is a derivative of imidazole and is commonly used in organic synthesis and pharmaceutical research. Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride has potential applications in drug development and research due to its ability to act as a building block for the synthesis of various biologically active compounds.

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  • 116401-54-8 Structure
  • Basic information

    1. Product Name: Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride
    2. Synonyms: Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride
    3. CAS NO:116401-54-8
    4. Molecular Formula: C5H7N3O2*ClH
    5. Molecular Weight: 177.58892
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116401-54-8.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: Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride(116401-54-8)
    11. EPA Substance Registry System: Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride(116401-54-8)
  • 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: 116401-54-8(Hazardous Substances Data)

116401-54-8 Usage

Uses

Used in Pharmaceutical Research:
Methyl 5-amino-1H-imidazole-4-carboxylate hydrochloride is used as a building block for the synthesis of various biologically active compounds, contributing to the development of new pharmaceutical drugs.
Used in Organic Synthesis:
Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride is utilized in organic synthesis processes, where it serves as a key intermediate for the creation of complex organic molecules.
Used in Drug Preparation:
Methyl 5-amino-1H-imidazole-4-carboxylate hydrochloride is used in the preparation of pharmaceutical drugs, playing a crucial role in the formulation and synthesis of medications.
Used as a Reagent in Chemical Reactions:
Methyl 5-aMino-1H-iMidazole-4-carboxylate hydrochloride also functions as a reagent in various chemical reactions, facilitating the transformation of other substances in the pursuit of new chemical entities and materials.
Methyl 5-amino-1H-imidazole-4-carboxylate hydrochloride is a valuable chemical in the field of medicinal chemistry and is the subject of ongoing research for potential therapeutic applications, making it an essential component in the advancement of healthcare and pharmaceutical innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 116401-54-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116401-54:
(8*1)+(7*1)+(6*6)+(5*4)+(4*0)+(3*1)+(2*5)+(1*4)=88
88 % 10 = 8
So 116401-54-8 is a valid CAS Registry Number.

116401-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-1(3)H-imidazole-4-carboxylic acid methyl ester, hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:116401-54-8 SDS

116401-54-8Downstream Products

116401-54-8Relevant articles and documents

SYNTHESIS AND PROPERTIES OF ANALOGS OF 5(4)-AMINOIMIDAZOLE-4(5)-CARBOXAMIDE AND PURINES. 15. RING OPENING IN IMIDAZO-1,2,3-TRIAZINES

Usova, V. K.,Selezneva, I. S.,Pospelova, T. A.,Mokrushin V. S.

, p. 1045 - 1047 (2007/10/02)

It has been shown that 4-methylthio-, ethoxy-, and methoxyimidazotriazines and imidazotriazin-4-ones, unlike benzo-1,2,3-triazines, do not display cryptodiazonium behavior.A novel type of fission of the triazine ring to give esters and thioesters of 5-aminoimidazole-4-carboxylic acid is described.

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