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183537-54-4

1,2,5-Oxadiazole-3-methanol, 4-amino-alpha-methyl-, 2-oxide (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183537-54-4 Structure

  • Basic information

    1. Product Name: 1,2,5-Oxadiazole-3-methanol, 4-amino-alpha-methyl-, 2-oxide (9CI)
    2. Synonyms: 1,2,5-Oxadiazole-3-methanol, 4-amino-alpha-methyl-, 2-oxide (9CI)
    3. CAS NO:183537-54-4
    4. Molecular Formula: C4H7N3O3
    5. Molecular Weight: 145.11668
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP;AMINEPRIMARY
    8. Mol File: 183537-54-4.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: 1,2,5-Oxadiazole-3-methanol, 4-amino-alpha-methyl-, 2-oxide (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,5-Oxadiazole-3-methanol, 4-amino-alpha-methyl-, 2-oxide (9CI)(183537-54-4)
    11. EPA Substance Registry System: 1,2,5-Oxadiazole-3-methanol, 4-amino-alpha-methyl-, 2-oxide (9CI)(183537-54-4)

  • 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: 183537-54-4(Hazardous Substances Data)

183537-54-4 Usage

Organic compound

Yes
It is an organic compound as it contains carbon and hydrogen atoms, along with other elements.

Heterocyclic ring

Present
The compound contains a heterocyclic ring, which is a ring of atoms with at least one atom not being carbon.

Amino group

Present
The compound has an amino group (-NH2), which is a functional group consisting of a nitrogen atom bonded to two hydrogen atoms.

Synonyms

4-Amino-alpha-methyl-1,2,5-oxadiazole-3-methanol 2-oxide
These are alternative names for the same chemical compound.

Physical state

White crystalline solid
The compound appears as a white crystalline solid at room temperature.

Molecular weight

130.104 g/mol
This is the mass of one mole of the compound, which is the sum of the atomic weights of all the atoms in the molecule.

Pharmaceutical research and synthesis

Used in
The compound is utilized in pharmaceutical research and synthesis due to its potential biological activities.

Applications

Medicinal chemistry and drug discovery
It may have applications in the field of medicinal chemistry and drug discovery due to its structural properties and potential pharmacological properties.

Biological activities

Potential
The compound has potential biological activities, which could be explored for therapeutic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 183537-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,5,3 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183537-54:
(8*1)+(7*8)+(6*3)+(5*5)+(4*3)+(3*7)+(2*5)+(1*4)=154
154 % 10 = 4
So 183537-54-4 is a valid CAS Registry Number.

183537-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-amino-2-oxido-1,2,5-oxadiazol-2-ium-3-yl)ethanol

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:183537-54-4 SDS

183537-54-4Upstream product

183537-54-4Downstream Products

183537-54-4Relevant articles and documents

α-Hydroxyalkyl(benzyl)furazans and α-hydroxyalkyl(benzyl)furoxans synthesis and reactivity

Blinnikov,Kulikov,Makhova,Khmel'nitskii

, p. 1692 - 1698 (2007/10/03)

A general and simple preparative method for the synthesis of α-hydroxyalkyl(benzyl)furazan and -furoxan derivatives is proposed. The method involves reduction of acyl or ethoxycarbonyl substituents in these heterocyclic compounds with NaBH4 in

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