Cas 362634-52-4,{(2R,3S)-3-[2-((S)-1-Dimethylamino-ethyl)-phenylselanyl]-tetrahydro-furan-2-yloxy}-acetic acid methyl ester

362634-52-4

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Basic information

Product Name: {(2R,3S)-3-[2-((S)-1-Dimethylamino-ethyl)-phenylselanyl]-tetrahydro-furan-2-yloxy}-acetic acid methyl ester
Synonyms:
CAS NO:362634-52-4
Molecular Formula:
Molecular Weight: 386.35
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: {(2R,3S)-3-[2-((S)-1-Dimethylamino-ethyl)-phenylselanyl]-tetrahydro-furan-2-yloxy}-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(2R,3S)-3-[2-((S)-1-Dimethylamino-ethyl)-phenylselanyl]-tetrahydro-furan-2-yloxy}-acetic acid methyl ester(362634-52-4)
EPA Substance Registry System: {(2R,3S)-3-[2-((S)-1-Dimethylamino-ethyl)-phenylselanyl]-tetrahydro-furan-2-yloxy}-acetic acid methyl ester(362634-52-4)

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: 362634-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 362634-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,2,6,3 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 362634-52:
(8*3)+(7*6)+(6*2)+(5*6)+(4*3)+(3*4)+(2*5)+(1*2)=144
144 % 10 = 4
So 362634-52-4 is a valid CAS Registry Number.

362634-52-4Upstream product

362634-52-4Downstream Products

362634-52-4Relevant academic research and scientific papers

Stereoselective synthesis of optically active perhydrofuro[2,3-b]furan derivatives

Uchiyama, Masahiko,Hirai, Manabu,Nagata, Momoko,Katoh, Rui,Ogawa, Risa,Ohta, Akihiro

, p. 4653 - 4656 (2001)

(1R,5S)-2,8-Dioxabicyclo[3.3.0]octan-3-one and its derivatives, important subunits in various biologically active natural products, have been synthesized based on a new approach using the asymmetric oxyselenenylation of 2,3-dihydrofuran as the key step.

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