Cas 201848-38-6,3-Benzyloxymethyl-1-[(1R,3S,4R)-3-benzyloxy-4-(3-oxo-1,5-dihydro-3λ<sup>5</sup>-benzo[e][1,3,2]dioxaphosphepin-3-yloxymethyl)-cyclopentyl]-5-methyl-1H-pyrimidine-2,4-dione

201848-38-6

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Product Name: 3-Benzyloxymethyl-1-[(1R,3S,4R)-3-benzyloxy-4-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxymethyl)-cyclopentyl]-5-methyl-1H-pyrimidine-2,4-dione
Synonyms:
CAS NO:201848-38-6
Molecular Formula:
Molecular Weight: 632.65
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: 3-Benzyloxymethyl-1-[(1R,3S,4R)-3-benzyloxy-4-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxymethyl)-cyclopentyl]-5-methyl-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-Benzyloxymethyl-1-[(1R,3S,4R)-3-benzyloxy-4-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxymethyl)-cyclopentyl]-5-methyl-1H-pyrimidine-2,4-dione(201848-38-6)
EPA Substance Registry System: 3-Benzyloxymethyl-1-[(1R,3S,4R)-3-benzyloxy-4-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxymethyl)-cyclopentyl]-5-methyl-1H-pyrimidine-2,4-dione(201848-38-6)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 201848-38-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201848-38-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,8,4 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 201848-38:
(8*2)+(7*0)+(6*1)+(5*8)+(4*4)+(3*8)+(2*3)+(1*8)=116
116 % 10 = 6
So 201848-38-6 is a valid CAS Registry Number.

201848-38-6Upstream product

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201848-38-6Relevant academic research and scientific papers

Synthesis of the optically active carbocyclic analogs of the four 2'- deoxyribonucleoslde monophosphates

Schmitt, Laurent,Caperelli, Carol A.

, p. 2165 - 2192 (2007/10/03)

The (+)-enantiomer of the carbocyclic analogs of the four 2'-deoxy- ribonucleoside monophosphate constituents of DNA, C-dAMP2 (1: A), C-dGMP (1: G), C-dCMP (1: C), and C-TMP (1: T) have been synthesized via the Mitsunobu coupling reaction. Two

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