Cas 870461-33-9,Methanesulfonic acid (1S,5S,8S,9S)-2-benzyl-8-(tert-butyl-dimethyl-silanyloxymethyl)-6,6-dimethyl-3,7-dioxa-2-aza-bicyclo[3.3.1]non-9-yl ester

870461-33-9

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Basic information

Product Name: Methanesulfonic acid (1S,5S,8S,9S)-2-benzyl-8-(tert-butyl-dimethyl-silanyloxymethyl)-6,6-dimethyl-3,7-dioxa-2-aza-bicyclo[3.3.1]non-9-yl ester
Synonyms: Methanesulfonic acid (1S,5S,8S,9S)-2-benzyl-8-(tert-butyl-dimethyl-silanyloxymethyl)-6,6-dimethyl-3,7-dioxa-2-aza-bicyclo[3.3.1]non-9-yl ester
CAS NO:870461-33-9
Molecular Formula:
Molecular Weight: 485.717
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: Methanesulfonic acid (1S,5S,8S,9S)-2-benzyl-8-(tert-butyl-dimethyl-silanyloxymethyl)-6,6-dimethyl-3,7-dioxa-2-aza-bicyclo[3.3.1]non-9-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid (1S,5S,8S,9S)-2-benzyl-8-(tert-butyl-dimethyl-silanyloxymethyl)-6,6-dimethyl-3,7-dioxa-2-aza-bicyclo[3.3.1]non-9-yl ester(870461-33-9)
EPA Substance Registry System: Methanesulfonic acid (1S,5S,8S,9S)-2-benzyl-8-(tert-butyl-dimethyl-silanyloxymethyl)-6,6-dimethyl-3,7-dioxa-2-aza-bicyclo[3.3.1]non-9-yl ester(870461-33-9)

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: 870461-33-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 870461-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,4,6 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 870461-33:
(8*8)+(7*7)+(6*0)+(5*4)+(4*6)+(3*1)+(2*3)+(1*3)=169
169 % 10 = 9
So 870461-33-9 is a valid CAS Registry Number.

870461-33-9Upstream product

870461-33-9Downstream Products

870461-33-9Relevant academic research and scientific papers

Synthesis of enantiopure carbohydrate mimetics by Lewis acid catalyzed rearrangement of 1,3-dioxolanyl-substituted 1,2-oxazines

Al-Harrasi, Ahmed,Reissig, Hans-Ulrich

, p. 6227 - 6231 (2007/10/03)

(Chemical Equation Presented) Under control: Lewis acids induce an unexpected rearrangement of 1,3-dioxolanyl-substituted 1,2-oxazines to provide bicyclic compounds in a stereocontrolled manner. They are precursors for enantiopure carbohydrate mimetics co

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