Cas 1433812-41-9,1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

1433812-41-9

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Basic information

Product Name: 1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione
Synonyms: 1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione
CAS NO:1433812-41-9
Molecular Formula:
Molecular Weight: 649.978
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: 1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione(1433812-41-9)
EPA Substance Registry System: 1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione(1433812-41-9)

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: 1433812-41-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1433812-41-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,3,8,1 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1433812-41:
(9*1)+(8*4)+(7*3)+(6*3)+(5*8)+(4*1)+(3*2)+(2*4)+(1*1)=139
139 % 10 = 9
So 1433812-41-9 is a valid CAS Registry Number.

1433812-41-9Upstream product

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1433812-81-7 1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

1433812-41-9Relevant academic research and scientific papers

Synthesis and solvatochromic fluorescence of biaryl pyrimidine nucleosides

Mata, Guillaume,Luedtke, Nathan W.

, p. 2462 - 2465 (2013/07/11)

Fluorescent pyrimidine analogs containing a fused biphenyl unit were prepared in high yields using stereoselective N-glycosylation and Suzuki-Miyaura cross-coupling reactions. The resulting push-pull fluorophores exhibit highly solvatochromic emissions from twisted intramolecular charge-transfer (TICT) states.

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