Cas 88867-00-9,methyl (N4-benzoyl-2'-O-t-butyldimethylsilyl)cytidylyl (3'-> 5') (N6,O2',O3'-tribenzoyl)adenosine

88867-00-9

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Basic information

Product Name: methyl (N⁴-benzoyl-2'-O-t-butyldimethylsilyl)cytidylyl (3'-> 5') (N⁶,O^2',O^3'-tribenzoyl)adenosine
Synonyms: methyl (N⁴-benzoyl-2'-O-t-butyldimethylsilyl)cytidylyl (3'-> 5') (N⁶,O^2',O^3'-tribenzoyl)adenosine
CAS NO:88867-00-9
Molecular Formula:
Molecular Weight: 1117.15
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: methyl (N⁴-benzoyl-2'-O-t-butyldimethylsilyl)cytidylyl (3'-> 5') (N⁶,O^2',O^3'-tribenzoyl)adenosine(CAS DataBase Reference)
NIST Chemistry Reference: methyl (N⁴-benzoyl-2'-O-t-butyldimethylsilyl)cytidylyl (3'-> 5') (N⁶,O^2',O^3'-tribenzoyl)adenosine(88867-00-9)
EPA Substance Registry System: methyl (N⁴-benzoyl-2'-O-t-butyldimethylsilyl)cytidylyl (3'-> 5') (N⁶,O^2',O^3'-tribenzoyl)adenosine(88867-00-9)

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: 88867-00-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88867-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,6 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88867-00:
(7*8)+(6*8)+(5*8)+(4*6)+(3*7)+(2*0)+(1*0)=189
189 % 10 = 9
So 88867-00-9 is a valid CAS Registry Number.

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88867-00-9Relevant academic research and scientific papers

PREPARATION OF 2'(3')-O-Acyl-pCpA DERIVATIVES AS SUBSTRATES FOR T4 RNA LIGASE-MEDIATED "CHEMICAL AMINOACILATION"

Heckler, T.G.,Chang, L.H.,Zama, Y.,Naka, T.,Hecht, S.M.

, p. 87 - 94 (1984)

The synthesis of 2'(3')-O-(amino)acyl-pCpA derivatives is described and the products are characterized chemically and as substrates for T4 RNA ligase in the presence of E.coli tRNAPhe-COH.The modified (N-acetylamino)acyl-tRNA's so derived are characterized by their chromatographic and biochemical properties, and by their ability to act as P-site t-RNA donors in the peptidyltransferase reaction.

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