Cas 851346-34-4,9-{2'-O-[(4'4''-dimethoxytriphenyl)methyl]-α-L-threofuranosyl}-2,6-diaminopurine

851346-34-4

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Basic information

Product Name: 9-{2'-O-[(4'4''-dimethoxytriphenyl)methyl]-α-L-threofuranosyl}-2,6-diaminopurine
Synonyms: 9-{2'-O-[(4'4''-dimethoxytriphenyl)methyl]-α-L-threofuranosyl}-2,6-diaminopurine
CAS NO:851346-34-4
Molecular Formula:
Molecular Weight: 554.605
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: 9-{2'-O-[(4'4''-dimethoxytriphenyl)methyl]-α-L-threofuranosyl}-2,6-diaminopurine(CAS DataBase Reference)
NIST Chemistry Reference: 9-{2'-O-[(4'4''-dimethoxytriphenyl)methyl]-α-L-threofuranosyl}-2,6-diaminopurine(851346-34-4)
EPA Substance Registry System: 9-{2'-O-[(4'4''-dimethoxytriphenyl)methyl]-α-L-threofuranosyl}-2,6-diaminopurine(851346-34-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 851346-34-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 851346-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,3,4 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 851346-34:
(8*8)+(7*5)+(6*1)+(5*3)+(4*4)+(3*6)+(2*3)+(1*4)=164
164 % 10 = 4
So 851346-34-4 is a valid CAS Registry Number.

851346-34-4Upstream product

425394-11-2 N²,N⁶-dibenzoyl-9-{2'-O-[(4,4'-dimethoxytriphenyl)methyl]-α-L-threofuranosyl}-2,6-diaminopurine

851346-34-4Downstream Products

851346-34-4Relevant academic research and scientific papers

Synthesis of α-L-threofuranosyl nucleoside triphosphates (tNTPs)

Zou, Keyong,Horhota, Allen,Yu, Biao,Szostak, Jack W.,McLaughlin, Larry W.

, p. 1485 - 1487 (2005)

(Chemical Equation Presented) The α-L-threofuranosyl nucleoside triphosphates of T, G, and D (tTTP, tGTP, and tDTP) were synthesized from the described 2′-O-DMT-protected derivatives using the Eckstein method, while the corresponding C derivative (tCTP) w

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