144660-79-7

• 

• Basic information

  1. Product Name: 4-methylamidatetiazofurin
  2. Synonyms: 4-methylamidatetiazofurin
  3. CAS NO:144660-79-7
  4. Molecular Formula: C10H14N2O5S
  5. Molecular Weight: 274.29356
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 144660-79-7.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 495.8°Cat760mmHg
  3. Flash Point: 253.6°C
  4. Appearance: /
  5. Density: 1.75g/cm³
  6. Vapor Pressure: 1.2E-10mmHg at 25°C
  7. Refractive Index: 1.714
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 4-methylamidatetiazofurin(CAS DataBase Reference)
  11. NIST Chemistry Reference: 4-methylamidatetiazofurin(144660-79-7)
  12. EPA Substance Registry System: 4-methylamidatetiazofurin(144660-79-7)

• 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: 144660-79-7(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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144660-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144660-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,6 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144660-79:
(8*1)+(7*4)+(6*4)+(5*6)+(4*6)+(3*0)+(2*7)+(1*9)=137
137 % 10 = 7
So 144660-79-7 is a valid CAS Registry Number.

InChI:InChI=1/C10H14N2O5S/c1-16-9(11)4-3-18-10(12-4)8-7(15)6(14)5(2-13)17-8/h3,5-8,11,13-15H,2H2,1H3/b11-9-/t5-,6-,7-,8-/m1/s1

144660-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	methyl 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-thiazole-4-carboximidate

1.2 Other means of identification

Product number	-
Other names	4-Methylamidatetiazofurin

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:144660-79-7 SDS

144660-79-7Upstream product

• 61502-39-4 2-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)thiazole-4-carbonitrile 
• 124-41-4 sodium methylate 
• 144660-78-6 4-cyanotiazofurin 

144660-79-7Downstream Products

144660-79-7Relevant articles and documents

Synthesis and antiviral (RNA) evaluation of nucleoside analogs of tiazofurin modified at the carboxamide moiety

Phelan,Gabrielsen,Kirsi,Shannon,Ussery,Barthel- Rosa,Schubert,Kini,Robins

, p. 1315 - 1327 (2007/10/02)

The carboxamide functionality of tiazofurin 1a has been modified to produce the following analogs: carboximidates 5a,b, carboxarnidines 6, 10, tetrahydropyrimidine 7, N-glycine 8 and N-glutamine 9. These structural modifications abolished the in vitro antiviral (RNA) activity exhibited by tiazofurin against the flaviviruses (yellow fever and Japanese encephalitis viruses), bunyavirus (Punta Toro virus) and togavirus (Venezuelan equine encephalomyelitis virus). Only carboximidates 5a,b retained marginal activity against bunyaviruses.

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