15676-19-4

• 

• Basic information

  1. Product Name: 4-amino-7-(2-deoxy-beta-D-erythro-pentofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile
  2. Synonyms:
  3. CAS NO:15676-19-4
  4. Molecular Formula: C₁₂H₁₃N₅O₃
  5. Molecular Weight: 275.2633
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15676-19-4.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 674.8°C at 760 mmHg
  3. Flash Point: 361.9°C
  4. Appearance: N/A
  5. Density: 1.77g/cm³
  6. Vapor Pressure: 3.95E-19mmHg at 25°C
  7. Refractive Index: 1.814
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 4-amino-7-(2-deoxy-beta-D-erythro-pentofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile(CAS DataBase Reference)
  11. NIST Chemistry Reference: 4-amino-7-(2-deoxy-beta-D-erythro-pentofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile(15676-19-4)
  12. EPA Substance Registry System: 4-amino-7-(2-deoxy-beta-D-erythro-pentofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile(15676-19-4)

• 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: 15676-19-4(Hazardous Substances Data)

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• SDS
• Upstream product
• Downstream Products
• Article

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• 7-Cyano-7-deaza-2'-deoxyadenosine

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• 7-Cyano-7-deaza-2'-deoxyadenosine

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• 4-amino-7-(2-deoxy-beta-D-erythro-pentofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile

  Cas No: 15676-19-4

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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15676-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15676-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,7 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15676-19:
(7*1)+(6*5)+(5*6)+(4*7)+(3*6)+(2*1)+(1*9)=124
124 % 10 = 4
So 15676-19-4 is a valid CAS Registry Number.

15676-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-amino-7-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrrolo[2,3-d]pyrimidine-5-carbonitrile

1.2 Other means of identification

Product number	-
Other names	2'-deoxytoyocamycin

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:15676-19-4 SDS

15676-19-4Upstream product

• 110089-46-8 4-amino-6-bromo-7-(2-deoxy-3,5-di-O-acetyl-β-D-erythro-pentofuranosyl)pyrrolo<2,3-d>-pyrimidine-5-carbonitrile 
• 98130-58-6 2-amino-5-bromo-1H-pyrrole-3,4-dicarbonitrile 
• 110089-47-9 4-amino-7-(2-deoxy-3,5-di-O-acetyl-β-D-erythro-pentofuranosyl)pyrrolo<2,3-d>pyrimidine-5-carbonitrile 
• 110089-45-7 4-amino-6-bromo-7-(2-deoxy-β-D-erythro-pentofuranosyl)pyrrolo<2,3-d>-pyrimidine-5-carbonitrile 
• 110089-43-5 2-bromo-5-(ethoxymethyleneamino)pyrrole-3,4-dicarbonitrile 
• 544-92-3 copper(I) cyanide 
• 166247-63-8 7-deaza-2'-deoxy-7-iodoadenosine 
• 85335-81-5 4-Amino-7-((2R,3aS,9aR)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile 
• 2179-92-2 tri-n-butyltin cyanide 

15676-19-4Downstream Products

• 83379-28-6 4-amino-5-carboxamido-7-(2-deoxy-β-D-erythro-pentofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine 
• 259244-23-0 5-cyano-7-[2-deoxy-5-O-(4,4'-dimethoxytriphenylmethyl)-β-D-erythro-pentofuranosyl]-4-{[(dimethylamino)-methylene]amino}-7H-pyrrolo[2,3-d]pyrimidine 

15676-19-4Relevant articles and documents

Incorporation of 2'-deoxysangivamycin in DNA duplexes: The conversion of a pyrrolo[2,3-d]pyrimidine nitrile to a carboxamide upon oligonucleotide deprotection

Seela, Frank,Zulauf, Matthias

, p. 2697 - 2709 (2007/10/03)

Oligonucleotides containing 2'-deoxysangivamycin are described. The phosphoramidite of 2'-deoxytoyocamycin was prepared and used in solid-phase synthesis. Upon deprotection the pyrrolo[2,3-d]pyrimidine nitrile residues were converted to carboxamides. Acco

NUCLEIC ACID RELATED COMPOUNDS. 42. A GENERAL PROCEDURE FOR THE EFFICIENT DEOXYGENATION OF SECONDARY ALCOHOLS. REGIOSPECIFIC AND STEREOSELECTIVE CONVERSION OF RIBONUCLEOSIDES TO 2 prime -DEOXYNUCLEOSIDES.

Robins,Wilson,Hansske

, p. 4059 - 4065 (2007/10/02)

Treatment of unhindered secondary alcohols with phenoxythiocarbonyl chloride (phenyl chlorothionocarbonate) in pyridine/dichloromethane, or in acetonitrile with 4-dimethylaminopyridine catalysis for hindered alcohols, gave clean conversion to their O-phenoxythiocarbonyl derivatives. Reductive deoxygenation of these phenyl thionocarbonate esters proceeded smoothly, using tri-n-butyltin hydride and a free radical initiator in warm toluene. Overall conversion yields ranged from 57 to 78% for the naturally occurring nucleosides, nucleoside antibiotics, and methyl beta -D-ribofuranoside.

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