151006-30-3

• 

• Basic information

  1. Product Name: (3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4-hydroxybutyl)phosphonic acid
  2. Synonyms: (3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4-hydroxybutyl)phosphonic acid
  3. CAS NO:151006-30-3
  4. Molecular Formula: C10H16 N5 O6 P
  5. Molecular Weight: 333.24
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 151006-30-3.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 794.6°Cat760mmHg
  3. Flash Point: 434.4°C
  4. Appearance: /
  5. Density: 1.94g/cm³
  6. Vapor Pressure: 1.27E-26mmHg at 25°C
  7. Refractive Index: 1.766
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: (3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4-hydroxybutyl)phosphonic acid(CAS DataBase Reference)
  11. NIST Chemistry Reference: (3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4-hydroxybutyl)phosphonic acid(151006-30-3)
  12. EPA Substance Registry System: (3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4-hydroxybutyl)phosphonic acid(151006-30-3)

• 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: 151006-30-3(Hazardous Substances Data)

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151006-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151006-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,0 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 151006-30:
(8*1)+(7*5)+(6*1)+(5*0)+(4*0)+(3*6)+(2*3)+(1*0)=73
73 % 10 = 3
So 151006-30-3 is a valid CAS Registry Number.

InChI:InChI=1/C10H16N5O6P/c11-10-13-8-7(9(17)14-10)12-4-15(8)5-21-6(3-16)1-2-22(18,19)20/h4,6,16H,1-3,5H2,(H2,18,19,20)(H3,11,13,14,17)/t6-/m1/s1

151006-30-3SDS

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	(3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4-hydroxybutyl)phosphonic acid

1.2 Other means of identification

Product number	-
Other names	1-PYRROLIDINECARBOXYLIC ACID VINYL ESTER

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:151006-30-3 SDS

151006-30-3Upstream product

• 150943-39-8 (R)-2-((2-acetamido-1,6-dihydro-6-oxo-7H-purin-7-yl)methoxy)-4-chlorobutyl benzoate 
• 150943-37-6 (R)-1-((tert-butyldiphenylsilyl)oxy)-4-chloro-2-(methoxymethoxy)butane 
• 150943-38-7 (R)-4-chloro-2-(methoxymethoxy)butyl benzoate 
• 3056-33-5 2,9-diacetylguanine 
• 266344-94-9 (R)-3-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)-4-hydroxybutylphosphonic acid monophosphate 
• 156721-88-9 (R)-diethyl <3-((2-acetamido-1,6-dihydro-6-oxo-7H-purin-7-yl)methoxy)-4-(benzoyloxy)butyl>phosphonate 

151006-30-3Downstream Products

151006-30-3Relevant articles and documents

Phosphorylation of ganciclovir phosphonate by cellular GMP kinase determines the stereoselectivity of anti-human cytomegalovirus activity

Miller, Wayne H.,Beauchamp, Lilia M.,Meade, Eric,Reardon, John E.,Biron, Karen K.,Smith, Albert A.,Goss, Charles A.,Miller, Richard L.

, p. 341 - 356 (2007/10/03)

A racemic mixture of ganciclovir phosphonate was resolved by stereoselective phosphorylation using GMP kinase. The R-enantiomer of ganciclovir phosphonate was active against human cytomegalovirus but the S- enantiomer was less active. We show that enantiomeric selectivity of antiviral activity for ganciclovir phosphonate was conferred by stereoselective phosphorylations by mammalian enzymes, not by stereoslective inhibition of DNA polymerase from human cytomegalovirus.

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