Cas 637035-77-9,(1S,2R,4R,5S)-2-Azidomethyl-4-p-tolylsulfanyl-3,6-dioxa-bicyclo[3.1.0]hexane

637035-77-9

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Basic information

Product Name: (1S,2R,4R,5S)-2-Azidomethyl-4-p-tolylsulfanyl-3,6-dioxa-bicyclo[3.1.0]hexane
Synonyms: (1S,2R,4R,5S)-2-Azidomethyl-4-p-tolylsulfanyl-3,6-dioxa-bicyclo[3.1.0]hexane
CAS NO:637035-77-9
Molecular Formula:
Molecular Weight: 263.32
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: (1S,2R,4R,5S)-2-Azidomethyl-4-p-tolylsulfanyl-3,6-dioxa-bicyclo[3.1.0]hexane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,4R,5S)-2-Azidomethyl-4-p-tolylsulfanyl-3,6-dioxa-bicyclo[3.1.0]hexane(637035-77-9)
EPA Substance Registry System: (1S,2R,4R,5S)-2-Azidomethyl-4-p-tolylsulfanyl-3,6-dioxa-bicyclo[3.1.0]hexane(637035-77-9)

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: 637035-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 637035-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,0,3 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 637035-77:
(8*6)+(7*3)+(6*7)+(5*0)+(4*3)+(3*5)+(2*7)+(1*7)=159
159 % 10 = 9
So 637035-77-9 is a valid CAS Registry Number.

637035-77-9Upstream product

204918-49-0 p-methylphenyl 1-thio-α-D-arabinofuranoside

637035-77-9Downstream Products

637035-73-5 (1S,2R,4R,5S)-2-Azidomethyl-4-(toluene-4-sulfinyl)-3,6-dioxa-bicyclo[3.1.0]hexane

637035-77-9Relevant academic research and scientific papers

An efficient route to pyrimidine nucleosides with the 2,3-anhydro-β-D-lyxofuranosyl stereochemistry

Callam, Christopher S.,Gadikota, Rajendrakumar Reddy,Lowary, Todd L.

, p. 1271 - 1274 (2003)

Described is the efficient preparation of 2,3-anhydro-β-D-lyxofuranosyl pyrimidine nucleosides via the coupling of a 2,3-anhydrosugar-containing glycosyl donor (5 or 6) with a silylated nucleoside base. The products are obtained with a high degree of stereoselectivity and in 65-77% yield.

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