Cas 355127-52-5,N-(S-trityl-2-mercaptoacetyl)-O-tert-butyldiphenylsilyl-3-aminopropanol

355127-52-5

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Basic information

Product Name: N-(S-trityl-2-mercaptoacetyl)-O-tert-butyldiphenylsilyl-3-aminopropanol
Synonyms: N-(S-trityl-2-mercaptoacetyl)-O-tert-butyldiphenylsilyl-3-aminopropanol
CAS NO:355127-52-5
Molecular Formula:
Molecular Weight: 629.938
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: N-(S-trityl-2-mercaptoacetyl)-O-tert-butyldiphenylsilyl-3-aminopropanol(CAS DataBase Reference)
NIST Chemistry Reference: N-(S-trityl-2-mercaptoacetyl)-O-tert-butyldiphenylsilyl-3-aminopropanol(355127-52-5)
EPA Substance Registry System: N-(S-trityl-2-mercaptoacetyl)-O-tert-butyldiphenylsilyl-3-aminopropanol(355127-52-5)

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: 355127-52-5(Hazardous Substances Data)

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355127-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 355127-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,1,2 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 355127-52:
(8*3)+(7*5)+(6*5)+(5*1)+(4*2)+(3*7)+(2*5)+(1*2)=135
135 % 10 = 5
So 355127-52-5 is a valid CAS Registry Number.

355127-52-5Upstream product

76-83-5 trityl chloride

355127-52-5Downstream Products

355127-53-6 N-(S-trityl-2-mercaptoacetyl)-3-aminopropanol

355127-52-5Relevant academic research and scientific papers

Synthesis and application of a novel, crystalline phosphoramidite monomer with thiol terminus, suitable for the synthesis of DNA conjugates

Kupihar, Zoltan,Schmel, Zoltan,Kele, Zoltan,Penke, Botond,Kovacs, Lajos

, p. 1241 - 1247 (2001)

A new, crystalline 5′-thiol modifier phosphoramidite monomer (3), suitable for DNA synthesis, has been prepared. This monomer has been built into an oligonucleotide using the standard protocol. After cleavage, purification and removal of the trityl group

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