105868-85-7

• 

• Basic information

  1. Product Name: 9-(4-hydroxy-2-(hydroxymethyl)butyl)guanine
  2. Synonyms: 9-(4-hydroxy-2-(hydroxymethyl)butyl)guanine;2-Amino-1,9-dihydro-9-[4-hydroxy-2-(hydroxymethyl)butyl]-6H-purin-6-one;2-Amino-9-[2-(hydroxymethyl)-4-hydroxybutyl]-6,9-dihydro-1H-purine-6-one;9-[4-Hydroxy-2-(hydroxymethyl)butyl]-2-amino-9H-purin-6(1H)-one
  3. CAS NO:105868-85-7
  4. Molecular Formula: C10H15 N5 O3
  5. Molecular Weight: 253.26
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 105868-85-7.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 637.8°C at 760 mmHg
  3. Flash Point: 339.5°C
  4. Appearance: /
  5. Density: 1.68g/cm³
  6. Vapor Pressure: 3.85E-17mmHg at 25°C
  7. Refractive Index: 1.748
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 9-(4-hydroxy-2-(hydroxymethyl)butyl)guanine(CAS DataBase Reference)
  11. NIST Chemistry Reference: 9-(4-hydroxy-2-(hydroxymethyl)butyl)guanine(105868-85-7)
  12. EPA Substance Registry System: 9-(4-hydroxy-2-(hydroxymethyl)butyl)guanine(105868-85-7)

• 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: 105868-85-7(Hazardous Substances Data)

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• 9-(4-hydroxy-2-(hydroxymethyl)butyl)guanine

  Cas No: 105868-85-7

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105868-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105868-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,6 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105868-85:
(8*1)+(7*0)+(6*5)+(5*8)+(4*6)+(3*8)+(2*8)+(1*5)=147
147 % 10 = 7
So 105868-85-7 is a valid CAS Registry Number.

InChI:InChI=1/C10H15N5O3/c11-10-13-8-7(9(18)14-10)12-5-15(8)3-6(4-17)1-2-16/h5-6,16-17H,1-4H2,(H3,11,13,14,18)

105868-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-amino-9-[4-hydroxy-2-(hydroxymethyl)butyl]-3H-purin-6-one

1.2 Other means of identification

Product number	-
Other names	2HM-Hbg

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:105868-85-7 SDS

105868-85-7Upstream product

• 112233-74-6 N₂-acetyl-O₆-(diphenylcarbamoyl)guanine 
• 126617-59-2 dimethyl 2-(2-amino-6-chloropurin-9-ylmethyl)-succinate 
• 121-43-7 Trimethyl borate 
• 67-56-1 methanol 
• 553646-42-7 ethyl 3-(2-N-acetyl-6-O-(diphenylcarbamoyl)guanin-9-ylmethyl)-2-(hydroxymethyl)propanoate 

105868-85-7Downstream Products

105868-85-7Relevant articles and documents

Rapid access to acyclic nucleosides via conjugate addition

Guillarme, Stéphane,Legoupy, Stéphanie,Aubertin, Anne-Marie,Olicard, Cécile,Bourgougnon, Nathalie,Huet, Fran?ois

, p. 2177 - 2184 (2007/10/03)

The synthesis of several acyclic nucleosides 5 and 6, analogs of penciclovir, was achieved by Michael addition as the key step. This reaction worked not only for the protected natural bases but even for the less nucleophilic deaza purine and deaza pyrimid

GUANINE DERIVATIVE

-

, (2008/06/13)

Antivirally active compounds of the formula STR1 wherein A is STR2 wherein m is 1 or 2, n is 1 or 2, whereby m is 1 when n is 2 and m is 2 when n is 1, R a ' is (CH 2) p OH, NHCONH 2 or COR a ", R a " is hydrogen, hydroxy or amino, p is 1 to 4, R b ' and R b " are independently selected from hydrogen or (CH 2) p OH, with the proviso that at least one of R b ' or R b " is hydrogen; or R b ' and R b " together constitute an additional carbon-carbon bond to form an alkyne; or a physiologically acceptable salt, geometric or optical isomer thereof; pharmaceutical preparations containing the compounds and methods for treatment of virus infections.

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