Cas 226256-00-4,3-S-(benzothiazol-2-yl)-1,2-O-isopropylidene-3-thio-5-O-trityl-α-D-xylofuranose

226256-00-4

Post Buying Request

Basic information

Product Name: 3-S-(benzothiazol-2-yl)-1,2-O-isopropylidene-3-thio-5-O-trityl-α-D-xylofuranose
Synonyms: 3-S-(benzothiazol-2-yl)-1,2-O-isopropylidene-3-thio-5-O-trityl-α-D-xylofuranose
CAS NO:226256-00-4
Molecular Formula:
Molecular Weight: 581.756
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: 3-S-(benzothiazol-2-yl)-1,2-O-isopropylidene-3-thio-5-O-trityl-α-D-xylofuranose(CAS DataBase Reference)
NIST Chemistry Reference: 3-S-(benzothiazol-2-yl)-1,2-O-isopropylidene-3-thio-5-O-trityl-α-D-xylofuranose(226256-00-4)
EPA Substance Registry System: 3-S-(benzothiazol-2-yl)-1,2-O-isopropylidene-3-thio-5-O-trityl-α-D-xylofuranose(226256-00-4)

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: 226256-00-4(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

226256-00-4 Suppliers

Recommended suppliers

226256-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226256-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,2,5 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 226256-00:
(8*2)+(7*2)+(6*6)+(5*2)+(4*5)+(3*6)+(2*0)+(1*0)=114
114 % 10 = 4
So 226256-00-4 is a valid CAS Registry Number.

226256-00-4Upstream product

226256-00-4Downstream Products

226256-00-4Relevant academic research and scientific papers

A new intramolecular migration in thiosugar chemistry: S → O transfer of a benzothiazol-2-yl group in saccharidic sulfones

Gueyrard, David,Lorin, Christelle,Moravcova, Jitka,Rollin, Patrick

, p. 317 - 331 (1999)

Saccharidic benzothiazol-2-yl sulfones - readily obtained through regioselective Mitsunobu thiofunctionalization followed by standard S-oxidation - can easily undergo benzothiazol-2-yl group S → O transfer when submitted to the action of a hindered base u

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 226256-00-4