Cas 169514-67-4,2-Amino-3-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-benzonitrile

169514-67-4

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Basic information

Product Name: 2-Amino-3-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-benzonitrile
Synonyms:
CAS NO:169514-67-4
Molecular Formula:
Molecular Weight: 532.639
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-Amino-3-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-benzonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-Amino-3-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-benzonitrile(169514-67-4)
EPA Substance Registry System: 2-Amino-3-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-benzonitrile(169514-67-4)

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: 169514-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 169514-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,5,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 169514-67:
(8*1)+(7*6)+(6*9)+(5*5)+(4*1)+(3*4)+(2*6)+(1*7)=164
164 % 10 = 4
So 169514-67-4 is a valid CAS Registry Number.

169514-67-4Upstream product

169514-67-4Downstream Products

169514-70-9 2-Amino-3-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-benzamide

169514-67-4Relevant academic research and scientific papers

Synthesis of quinazoline C-nucleosides: A new class of 6:6 bicyclic purine-like analogues

Sarma,Wilson,Otter,Klein

, p. 397 - 400 (1995)

The quinazoline C-nucleoside congeners of adenosine (1) and inosine (2) have been obtained by radical-induced addition of 4-bromobutyronitrile to C- ribosyl acrylonitrile 10. A base-catalyzed Ziegler-Thorpe cyclization of the dinitrile thus obtained (11)

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