Welcome to LookChem.com Sign In|Join Free

CAS

  • or

87614-68-4

Post Buying Request

87614-68-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

87614-68-4 Usage

Molecular structure

Contains an imidazole ring and a carbamide group, as well as an amino and hydrazino group

Potential use in pharmaceuticals

Presence of the imidazole ring suggests potential biological activity

Reactivity with other compounds

Presence of the amino and hydrazino groups could indicate potential reactivity with other chemical compounds

Further research required

More analysis and research needed to fully understand the properties and potential applications of this chemical

Check Digit Verification of cas no

The CAS Registry Mumber 87614-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,1 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87614-68:
(7*8)+(6*7)+(5*6)+(4*1)+(3*4)+(2*6)+(1*8)=164
164 % 10 = 4
So 87614-68-4 is a valid CAS Registry Number.

87614-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-5-amino-2-[(5-carbamoyl-1H-imidazol-4-yl)hydrazinylidene]imidazole-4-carboxamide

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:87614-68-4 SDS

87614-68-4Downstream Products

87614-68-4Relevant articles and documents

Antitumor Imidazotetrazines. 1. Synthesis and Chemistry of 8-Carbamoyl-3-(2-chloroethyl)imidazo-1,2,3,5-tetrazin-4(3H)-one, a Novel Broad-Spectrum Antitumor Agent

Stevens, Malcolm F. G.,Hickman, John A.,Stone, Robert,Gibson, Neil W.,Baig, Ghouse Unissa,et al.

, p. 196 - 201 (2007/10/02)

Interaction of 5-diazoimidazole-4-carboxamide and alkyl and aryl isocyanates in the dark affords 8-carbamoyl-3-substituted-imidazo-1,2,3,5-tetrazin-4(3H)-ones.In cold methanol or ethanol, the 3-(2-chloroethyl) derivative 7a decomposes to afford 2-azahypoxanthine (14) and methyl and ethyl N-(2-chloroethyl)carbamates, respectively.Compound 7a has curative activity against L-1210 and P388 leukemia and may act as a prodrug modification of the acyclic triazene 5-imidazole-4-carboxamide (MCTIC), since it ring opens to form the triazene in aqueous sodium carbonate.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 87614-68-4