Cas 183606-18-0,Methanesulfonic acid (1S,2S)-3-methanesulfonyloxy-2-(tetrahydro-pyran-2-yloxy)-1-trityloxymethyl-propyl ester

183606-18-0

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Basic information

Product Name: Methanesulfonic acid (1S,2S)-3-methanesulfonyloxy-2-(tetrahydro-pyran-2-yloxy)-1-trityloxymethyl-propyl ester
Synonyms: Methanesulfonic acid (1S,2S)-3-methanesulfonyloxy-2-(tetrahydro-pyran-2-yloxy)-1-trityloxymethyl-propyl ester
CAS NO:183606-18-0
Molecular Formula:
Molecular Weight: 604.742
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: Methanesulfonic acid (1S,2S)-3-methanesulfonyloxy-2-(tetrahydro-pyran-2-yloxy)-1-trityloxymethyl-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid (1S,2S)-3-methanesulfonyloxy-2-(tetrahydro-pyran-2-yloxy)-1-trityloxymethyl-propyl ester(183606-18-0)
EPA Substance Registry System: Methanesulfonic acid (1S,2S)-3-methanesulfonyloxy-2-(tetrahydro-pyran-2-yloxy)-1-trityloxymethyl-propyl ester(183606-18-0)

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: 183606-18-0(Hazardous Substances Data)

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183606-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183606-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,6,0 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 183606-18:
(8*1)+(7*8)+(6*3)+(5*6)+(4*0)+(3*6)+(2*1)+(1*8)=140
140 % 10 = 0
So 183606-18-0 is a valid CAS Registry Number.

183606-18-0Upstream product

183606-18-0Downstream Products

183606-17-9 2-((2R,3S)-2-Trityloxymethyl-thietan-3-yloxy)-tetrahydro-pyran

183606-18-0Relevant academic research and scientific papers

Nucleosides and nucleotides. 159. Synthesis of thietane nucleosides via the Pummerer reaction as a key step

Nishizono, Naozumi,Koike, Nobuaki,Yamagata, Yuriko,Fujii, Satoshi,Matsuda, Akira

, p. 7569 - 7572 (1996)

New thymine thietane nucleosides 7 and 20 were synthesized via Pummerer rearrangement of the corresponding sulfoxides 5 and 18 in the presence of thymine. TMSOTf, Et3N, and ZnI2 as a key step.

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