Cas 222992-24-7,5'-benzoylthiourea-3-(9-fluorenylmethoxycarbamoyl)-3',5'-deoxythymidine

222992-24-7

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Basic information

Product Name: 5'-benzoylthiourea-3-(9-fluorenylmethoxycarbamoyl)-3',5'-deoxythymidine
Synonyms: 5'-benzoylthiourea-3-(9-fluorenylmethoxycarbamoyl)-3',5'-deoxythymidine
CAS NO:222992-24-7
Molecular Formula:
Molecular Weight: 625.705
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: 5'-benzoylthiourea-3-(9-fluorenylmethoxycarbamoyl)-3',5'-deoxythymidine(CAS DataBase Reference)
NIST Chemistry Reference: 5'-benzoylthiourea-3-(9-fluorenylmethoxycarbamoyl)-3',5'-deoxythymidine(222992-24-7)
EPA Substance Registry System: 5'-benzoylthiourea-3-(9-fluorenylmethoxycarbamoyl)-3',5'-deoxythymidine(222992-24-7)

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: 222992-24-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 222992-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,9,9 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 222992-24:
(8*2)+(7*2)+(6*2)+(5*9)+(4*9)+(3*2)+(2*2)+(1*4)=137
137 % 10 = 7
So 222992-24-7 is a valid CAS Registry Number.

222992-24-7Upstream product

28920-43-6 (fluorenylmethoxy)carbonyl chloride

222992-24-7Downstream Products

222992-24-7Relevant academic research and scientific papers

Solid-phase synthesis of deoxynucleic guanidine (DNG) oligomersand melting point and circular dichroism analysis of binding fidelity of octameric thymidyl oligomers with DNA oligomers

Linkletter, Barry A.,Szabo, Istvan E.,Bruice, Thomas C.

, p. 3888 - 3896 (1999)

A practical solid-phase synthesis of deoxynucleic guanidine (DNG), a positively charged DNA backbone analogue, is reported. The nucleoside coupling step in the solid-phase synthesis of DNG involves the attack of a terminal 3′-amine upon an electronically

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