Cas 909566-38-7,3',5'-O-bis(tert-butyldimethylsilyl)-4-N-[N-(phenylsulfonyl)carbamoyl]deoxycytidine

909566-38-7

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Basic information

Product Name: 3',5'-O-bis(tert-butyldimethylsilyl)-4-N-[N-(phenylsulfonyl)carbamoyl]deoxycytidine
Synonyms: 3',5'-O-bis(tert-butyldimethylsilyl)-4-N-[N-(phenylsulfonyl)carbamoyl]deoxycytidine
CAS NO:909566-38-7
Molecular Formula:
Molecular Weight: 638.933
EINECS: N/A
Product Categories: N/A
Mol File: 909566-38-7.mol
Article Data: 1

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',5'-O-bis(tert-butyldimethylsilyl)-4-N-[N-(phenylsulfonyl)carbamoyl]deoxycytidine(CAS DataBase Reference)
NIST Chemistry Reference: 3',5'-O-bis(tert-butyldimethylsilyl)-4-N-[N-(phenylsulfonyl)carbamoyl]deoxycytidine(909566-38-7)
EPA Substance Registry System: 3',5'-O-bis(tert-butyldimethylsilyl)-4-N-[N-(phenylsulfonyl)carbamoyl]deoxycytidine(909566-38-7)

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: 909566-38-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 909566-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,5,6 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 909566-38:
(8*9)+(7*0)+(6*9)+(5*5)+(4*6)+(3*6)+(2*3)+(1*8)=207
207 % 10 = 7
So 909566-38-7 is a valid CAS Registry Number.

909566-38-7Upstream product

909566-38-7Downstream Products

909566-38-7Relevant articles and documents

New thermolytic carbamoyl groups for the protection of nucleobases

Ohkubo, Akihiro,Kasuya, Rintaro,Miyata, Kenichi,Tsunoda, Hirosuke,Seio, Kohji,Sekine, Mitsuo

experimental part, p. 687 - 694 (2009/06/20)

It was found that N-arylcarbamoyl and N-(phenylsulfonyl)carbamoyl (psc) groups could be effectively introduced onto the amino groups of deoxycytidine and deoxyadenosine derivatives and could be removed thermolytically. We succeeded in synthesizing DNA pro

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