108742-10-5

• 

• Basic information

  1. Product Name: (1S,2S,3R,5R)-3-(2,6-diamino-9H-purin-9-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol
  2. Synonyms:
  3. CAS NO:108742-10-5
  4. Molecular Formula: C₁₁H₁₆N₆O₃
  5. Molecular Weight: 280.2831
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 108742-10-5.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 705°C at 760 mmHg
  3. Flash Point: 380.2°C
  4. Appearance: N/A
  5. Density: 2.08g/cm³
  6. Vapor Pressure: 7.31E-21mmHg at 25°C
  7. Refractive Index: 1.952
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: (1S,2S,3R,5R)-3-(2,6-diamino-9H-purin-9-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol(CAS DataBase Reference)
  11. NIST Chemistry Reference: (1S,2S,3R,5R)-3-(2,6-diamino-9H-purin-9-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol(108742-10-5)
  12. EPA Substance Registry System: (1S,2S,3R,5R)-3-(2,6-diamino-9H-purin-9-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol(108742-10-5)

• 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: 108742-10-5(Hazardous Substances Data)

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• SDS
• Upstream product
• Downstream Products
• Article

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108742-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108742-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,4 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 108742-10:
(8*1)+(7*0)+(6*8)+(5*7)+(4*4)+(3*2)+(2*1)+(1*0)=115
115 % 10 = 5
So 108742-10-5 is a valid CAS Registry Number.

108742-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	(1S,2S,3R,5R)-3-(2,6-diaminopurin-9-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol

1.2 Other means of identification

Product number	-
Other names	1,2-Cyclopentanediol,3-(2,6-diamino-9H-purin-9-yl)-5-(hydroxymethyl)-,rel-(1S,2S,3R,5R)

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:108742-10-5 SDS

108742-10-5Upstream product

• 108742-07-0 (+/-)-(1α,2β,3α,5α)-3-<(2,5-diamino-6-chloro-4-pyrimidyl)amino>-5-(hydroxymethyl)-1,2-cyclopentanediol 
• 108742-05-8 (+/-)-(1α,2β,3α,5α)-3-<(2-amino-6-chloro-4-pyrimidinyl)amino>-5-(hydroxymethyl)-1,2-cyclopentanediol 
• 50619-39-1 (1S,2R,3S,5S)-3-(2,5-Diamino-6-chloro-pyrimidin-4-ylamino)-5-hydroxymethyl-cyclopentane-1,2-diol 
• 88852-57-7 (1α,2α,3β,5β)-(+/-)-3-(2-amino-6-chloro-9H-purin-9-yl)-5-(hydroxymethyl)-1,2-cyclopentanediol 
• 108742-06-9 (+/-)-(1α,2β,3α,5α)-3-<<2-amino-6-chloro-5-<(4-chlorophenyl)azo>-4-pyrimidyl>amino>-5-(hydroxymethyl)-1,2-cyclopentanediol 
• 91382-82-0 (+/-)-(1α,2β,3α,5α)-3-amino-5-(hydroxymethyl)-1,2-cyclopentanediol 

108742-10-5Downstream Products

108742-10-5Relevant articles and documents

Synthesis and antiviral activity of carbocyclic analogues of xylofuranosides of 2-amino-6-substituted-purines and 2-amino-6-substituted-8-azapurines

Vince,Turakhia,Shannon,Arnett

, p. 2026 - 2030 (2007/10/02)

(±)-(1α,2β,3α,5α)-3-[(2,5-Diamino-6-chloro-4-pyrimidinyl)amino] -5-(hydroxmethyl)-1,2-cyclopentanediol (7) was synthesized from 2-amino-4,6-dichloropyrimidine and the carbocyclic xylofuranosylamine (±)-(1α,2β,3α,5α)-3-amino-5-(hydroxymethyl)-1,2-cyclopentanediol (2) by subsequent preparation of the 5-[(4-chlorophenyl)azo] derivative of the resulting pyrimidine and reduction of the azo moiety with zinc and acetic acid. The carbocyclic analogue of 2-amino-4-chloropurine xylofuranoside (8) and the corresponding 8-azapurine 11 were prepared from 7. The carbocyclic analogues xylofuranosylguanine (9), xylofuranosyl-2,6-diaminopurine (10), xylofuranosyl-8-azaguanine (13), and xylofuranosyl-8-aza-2,6-diaminopurine (14) were prepared from 8 and 11. Compounds 9 and 13 were active against herpes simplex virus (types 1 and 2), with 9 being the more potent against both viruses. Analogues 9 also exhibited potent activity against human cytomegalovirus and varicella-zoster virus.

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