Cas 18423-29-5,Ethyl 2,3,4,6-Tetradeoxy-4-dimethylamino-α-D-threo-hexopyranoside-Hydrogen p-Toluenesulfonate

18423-29-5

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Basic information

Product Name: Ethyl 2,3,4,6-Tetradeoxy-4-dimethylamino-α-D-threo-hexopyranoside-Hydrogen p-Toluenesulfonate
Synonyms: Ethyl 2,3,4,6-Tetradeoxy-4-dimethylamino-α-D-threo-hexopyranoside-Hydrogen p-Toluenesulfonate
CAS NO:18423-29-5
Molecular Formula:
Molecular Weight: 359.487
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: Ethyl 2,3,4,6-Tetradeoxy-4-dimethylamino-α-D-threo-hexopyranoside-Hydrogen p-Toluenesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: Ethyl 2,3,4,6-Tetradeoxy-4-dimethylamino-α-D-threo-hexopyranoside-Hydrogen p-Toluenesulfonate(18423-29-5)
EPA Substance Registry System: Ethyl 2,3,4,6-Tetradeoxy-4-dimethylamino-α-D-threo-hexopyranoside-Hydrogen p-Toluenesulfonate(18423-29-5)

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: 18423-29-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 18423-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,2 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18423-29:
(7*1)+(6*8)+(5*4)+(4*2)+(3*3)+(2*2)+(1*9)=105
105 % 10 = 5
So 18423-29-5 is a valid CAS Registry Number.

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18423-29-5Relevant academic research and scientific papers

Stereospecific Syntheses of D-Ossamine and D-Tolyposamine

Malik, Abdul,Afza, Nighat,Voelter, Wolfgang

, p. 636 - 640 (2007/10/02)

2,3,4,6-Tetradeoxy-4-(dimethylamino)-D-threo-hexose (D-ossamine, 7), the amino sugar fragment from the fungal metabolite ossamycin, and 4-amino-2,3,4,6-tetradeoxy-D-erythro-hexose (D-tolyposamine, 12), the enantiomeric constituent of the antibiotic tolypomycin, have been synthesized from D-glucose via hex-2-enopyranosides.

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