Cas 1266098-30-9,2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine

1266098-30-9

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Basic information

Product Name: 2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine
Synonyms: 2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine
CAS NO:1266098-30-9
Molecular Formula:
Molecular Weight: 634.978
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: 2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine(CAS DataBase Reference)
NIST Chemistry Reference: 2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine(1266098-30-9)
EPA Substance Registry System: 2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine(1266098-30-9)

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: 1266098-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1266098-30-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,6,0,9 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1266098-30:
(9*1)+(8*2)+(7*6)+(6*6)+(5*0)+(4*9)+(3*8)+(2*3)+(1*0)=169
169 % 10 = 9
So 1266098-30-9 is a valid CAS Registry Number.

1266098-30-9Upstream product

1266098-30-9Downstream Products

4291-63-8 2-chloro-2'-deoxyadenosine

1266098-30-9Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF CLADRIBINE

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Page/Page column 29-30, (2011/04/13)

A process for the preparation of cladribine of API grade is provided by direct coupling of O-protected 2-deoxy-ribofuranose with silylated 2-chloroadenine followed by deprotection of the resultant protected nucleoside in a separate step and then a purification step. Following the coupling, the desired N-9-glycosylated β-anomer of the nucleoside is directly isolated as a solid from the coupling reaction mixture by filtration in relatively high purity and yield, and it does not require purification.

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