Cas 80971-35-3,3'-O-(tert-butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxy-5-methylcytidine

80971-35-3

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Basic information

Product Name: 3'-O-(tert-butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxy-5-methylcytidine
Synonyms: 3'-O-(tert-butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxy-5-methylcytidine
CAS NO:80971-35-3
Molecular Formula:
Molecular Weight: 657.882
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'-O-(tert-butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxy-5-methylcytidine(CAS DataBase Reference)
NIST Chemistry Reference: 3'-O-(tert-butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxy-5-methylcytidine(80971-35-3)
EPA Substance Registry System: 3'-O-(tert-butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxy-5-methylcytidine(80971-35-3)

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: 80971-35-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80971-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,7 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80971-35:
(7*8)+(6*0)+(5*9)+(4*7)+(3*1)+(2*3)+(1*5)=143
143 % 10 = 3
So 80971-35-3 is a valid CAS Registry Number.

80971-35-3Upstream product

80971-34-2 3'-O-t-butyldimethylsilyl-5'-O-dimethoxytrityl-1-[5-methyl-4-triazolylpyrimidin-2(1H)-onyl]-β-D-2'-deoxyriboside

80971-35-3Downstream Products

80971-35-3Relevant academic research and scientific papers

Photosensitized [2 + 2] cycloaddition of N-acetylated cytosine affords stereoselective formation of cyclobutane pyrimidine dimer

Yamamoto, Junpei,Nishiguchi, Kosuke,Manabe, Koichiro,Masutani, Chikahide,Hanaoka, Fumio,Iwai, Shigenori

, p. 1165 - 1175 (2011)

Photocycloaddition between two adjacent bases in DNA produces a cyclobutane pyrimidine dimer (CPD), which is one of the major UV-induced DNA lesions, with either the cis-syn or trans-syn structure. In this study, we investigated the photosensitized intram

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