Cas 1173883-19-6,5'-O-dimethoxytritylthymidine 3'-O-[(5-nitro-2-thienyl)methyl-N,N-diisopropylphosphoramidite]

1173883-19-6

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Basic information

Product Name: 5'-O-dimethoxytritylthymidine 3'-O-[(5-nitro-2-thienyl)methyl-N,N-diisopropylphosphoramidite]
Synonyms: 5'-O-dimethoxytritylthymidine 3'-O-[(5-nitro-2-thienyl)methyl-N,N-diisopropylphosphoramidite]
CAS NO:1173883-19-6
Molecular Formula:
Molecular Weight: 832.912
EINECS: N/A
Product Categories: N/A
Mol File: 1173883-19-6.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: 5'-O-dimethoxytritylthymidine 3'-O-[(5-nitro-2-thienyl)methyl-N,N-diisopropylphosphoramidite](CAS DataBase Reference)
NIST Chemistry Reference: 5'-O-dimethoxytritylthymidine 3'-O-[(5-nitro-2-thienyl)methyl-N,N-diisopropylphosphoramidite](1173883-19-6)
EPA Substance Registry System: 5'-O-dimethoxytritylthymidine 3'-O-[(5-nitro-2-thienyl)methyl-N,N-diisopropylphosphoramidite](1173883-19-6)

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: 1173883-19-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1173883-19-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,8,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1173883-19:
(9*1)+(8*1)+(7*7)+(6*3)+(5*8)+(4*8)+(3*3)+(2*1)+(1*9)=176
176 % 10 = 6
So 1173883-19-6 is a valid CAS Registry Number.

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1173883-19-6Relevant articles and documents

The design, synthesis and evaluation of hypoxia-activated pro-oligonucleotides

Zhang, Nan,Tan, Chunyan,Cai, Puqin,Zhang, Peizhuo,Zhao, Yufen,Jiang, Yuyang

supporting information; experimental part, p. 3216 - 3218 (2009/12/01)

Hypoxia-activated pro-oligonucleotides were synthesized through the commercial phosphoramidite method, and could be readily cleaved to form normal oligos with good hypoxia selectivity in vitro under the effect of reductases, as well as in tumor cell extra

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