Cas 275812-99-2,Acetic acid (R)-2-[(4R,5R)-5-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(toluene-4-sulfonylamino)-ethyl ester

275812-99-2

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Basic information

Product Name: Acetic acid (R)-2-[(4R,5R)-5-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(toluene-4-sulfonylamino)-ethyl ester
Synonyms: Acetic acid (R)-2-[(4R,5R)-5-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(toluene-4-sulfonylamino)-ethyl ester
CAS NO:275812-99-2
Molecular Formula:
Molecular Weight: 417.48
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: Acetic acid (R)-2-[(4R,5R)-5-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(toluene-4-sulfonylamino)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (R)-2-[(4R,5R)-5-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(toluene-4-sulfonylamino)-ethyl ester(275812-99-2)
EPA Substance Registry System: Acetic acid (R)-2-[(4R,5R)-5-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(toluene-4-sulfonylamino)-ethyl ester(275812-99-2)

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: 275812-99-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 275812-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,5,8,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 275812-99:
(8*2)+(7*7)+(6*5)+(5*8)+(4*1)+(3*2)+(2*9)+(1*9)=172
172 % 10 = 2
So 275812-99-2 is a valid CAS Registry Number.

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275812-99-2Relevant academic research and scientific papers

Use of the N-tosyl-activated aziridine 1,2-dideoxy-1,2-iminomannitol as a synthon for 1-deoxymannojirimycin analogues

Joly, Gert J.,Peeters, Koen,Mao, Hua,Brossette, Thierry,Hoornaert, Georges J.,Compernolle, Frans

, p. 2223 - 2226 (2007/10/03)

1-Amino-1-deoxy-D-glucitol was converted into the selectively protected title compound 4, an N-tosyl-activated aziridine that readily underwent ring opening with various nucleophiles. Further deprotection of the 5,6-diol moiety followed by ring closure under Mitsunobu conditions afforded the corresponding 6-substituted analogues of 1-deoxymannojirimycin. (C) 2000 Elsevier Science Ltd.

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