Cas 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

259244-23-0

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Basic information

Product Name: 5-cyano-7-[2-deoxy-5-O-(4,4'-dimethoxytriphenylmethyl)-β-D-erythro-pentofuranosyl]-4-{[(dimethylamino)-methylene]amino}-7H-pyrrolo[2,3-d]pyrimidine
Synonyms:
CAS NO:259244-23-0
Molecular Formula:
Molecular Weight: 632.719
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-cyano-7-[2-deoxy-5-O-(4,4'-dimethoxytriphenylmethyl)-β-D-erythro-pentofuranosyl]-4-{[(dimethylamino)-methylene]amino}-7H-pyrrolo[2,3-d]pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 5-cyano-7-[2-deoxy-5-O-(4,4'-dimethoxytriphenylmethyl)-β-D-erythro-pentofuranosyl]-4-{[(dimethylamino)-methylene]amino}-7H-pyrrolo[2,3-d]pyrimidine(259244-23-0)
EPA Substance Registry System: 5-cyano-7-[2-deoxy-5-O-(4,4'-dimethoxytriphenylmethyl)-β-D-erythro-pentofuranosyl]-4-{[(dimethylamino)-methylene]amino}-7H-pyrrolo[2,3-d]pyrimidine(259244-23-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 259244-23-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 259244-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,2,4 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 259244-23:
(8*2)+(7*5)+(6*9)+(5*2)+(4*4)+(3*4)+(2*2)+(1*3)=150
150 % 10 = 0
So 259244-23-0 is a valid CAS Registry Number.

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259244-23-0Relevant academic research and scientific papers

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 (1999)

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

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