Cas 68354-56-3,Toluene-4-sulfonic acid (1S,2S,3S,4R,5R)-2-amino-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester

68354-56-3

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Basic information

Product Name: Toluene-4-sulfonic acid (1S,2S,3S,4R,5R)-2-amino-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester
Synonyms: Toluene-4-sulfonic acid (1S,2S,3S,4R,5R)-2-amino-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester
CAS NO:68354-56-3
Molecular Formula:
Molecular Weight: 315.347
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: Toluene-4-sulfonic acid (1S,2S,3S,4R,5R)-2-amino-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (1S,2S,3S,4R,5R)-2-amino-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester(68354-56-3)
EPA Substance Registry System: Toluene-4-sulfonic acid (1S,2S,3S,4R,5R)-2-amino-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester(68354-56-3)

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: 68354-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 68354-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,5 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68354-56:
(7*6)+(6*8)+(5*3)+(4*5)+(3*4)+(2*5)+(1*6)=153
153 % 10 = 3
So 68354-56-3 is a valid CAS Registry Number.

68354-56-3Upstream product

213594-48-0 1,6-Anhydro-4-benzylamino-4-deoxy-2-O-(4-methylbenzenesulfonyl)-β-D-glucopyranose

68354-56-3Downstream Products

68354-56-3Relevant academic research and scientific papers

Selective N-debenzylation of benzylamino derivatives of 1,6-anhydro-β-D-hexopyranoses

Kroutil, Jiri,Trnka, Tomas,Cerny, Miloslav

, p. 1681 - 1683 (2000)

(matrix presented) When the series of 2-, 3-, and 4-(benzylamino)-2-, 3-, and 4-deoxy derivatives of 1,6-anhydro-β-D-hexopyranoses in the D-gluco, D-lyxo, and D-arabino configurations were reacted with diisopropyl azodicarboxylate, N-benzyl groups were selectively cleaved in the presence of O-benzyl groups. The yields ranged from 51 to 97percent. The debenzylation of some aliphatic benzylamines is also discussed.

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