Cas 95087-08-4,1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-methoxy-1H-pyrazolo<3,4-d>pyrimidine

95087-08-4

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Basic information

Product Name: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-methoxy-1H-pyrazolo<3,4-d>pyrimidine
Synonyms: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-methoxy-1H-pyrazolo<3,4-d>pyrimidine
CAS NO:95087-08-4
Molecular Formula:
Molecular Weight: 266.257
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: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-methoxy-1H-pyrazolo<3,4-d>pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-methoxy-1H-pyrazolo<3,4-d>pyrimidine(95087-08-4)
EPA Substance Registry System: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-methoxy-1H-pyrazolo<3,4-d>pyrimidine(95087-08-4)

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: 95087-08-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95087-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,8 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95087-08:
(7*9)+(6*5)+(5*0)+(4*8)+(3*7)+(2*0)+(1*8)=154
154 % 10 = 4
So 95087-08-4 is a valid CAS Registry Number.

95087-08-4Upstream product

5399-92-8 4-chloro-1H-pyrazolo[3,4-d]pyrimidine

95087-08-4Downstream Products

17318-21-7 4-amino-1-(2-deoxy-β-D-erythro-pentofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine

95087-08-4Relevant academic research and scientific papers

SYNTHESIS OF 2'-DEOXYRIBONUCLEOSIDES OF ALLOPURINOL BY PHASE-TRANSFER GLYCOSYLATION

Seela, F.,Steker, H.

, p. 5017 - 5018 (1984)

Regioselective glycosylation of 4-methoxy-1H-pyrazolopyrimidine (6b) with the halogenose 7 was achieved by employing phase-transfer techniques.The N-1 glycosylation product 3a was formed in preponderance.It was converted into the allopurinol β-D-2'-deoxyribonucleoside 2.

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