Cas 1133982-01-0,4-O-tert-butyldimethylsilyl-3-O-(N-2,4-dimethoxybenzyl)carbamoyl-6-O-p-toluenesulfonyl-D-glucal

1133982-01-0

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Basic information

Product Name: 4-O-tert-butyldimethylsilyl-3-O-(N-2,4-dimethoxybenzyl)carbamoyl-6-O-p-toluenesulfonyl-D-glucal
Synonyms: 4-O-tert-butyldimethylsilyl-3-O-(N-2,4-dimethoxybenzyl)carbamoyl-6-O-p-toluenesulfonyl-D-glucal
CAS NO:1133982-01-0
Molecular Formula:
Molecular Weight: 607.797
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: 4-O-tert-butyldimethylsilyl-3-O-(N-2,4-dimethoxybenzyl)carbamoyl-6-O-p-toluenesulfonyl-D-glucal(CAS DataBase Reference)
NIST Chemistry Reference: 4-O-tert-butyldimethylsilyl-3-O-(N-2,4-dimethoxybenzyl)carbamoyl-6-O-p-toluenesulfonyl-D-glucal(1133982-01-0)
EPA Substance Registry System: 4-O-tert-butyldimethylsilyl-3-O-(N-2,4-dimethoxybenzyl)carbamoyl-6-O-p-toluenesulfonyl-D-glucal(1133982-01-0)

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: 1133982-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1133982-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,9,8 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1133982-01:
(9*1)+(8*1)+(7*3)+(6*3)+(5*9)+(4*8)+(3*2)+(2*0)+(1*1)=140
140 % 10 = 0
So 1133982-01-0 is a valid CAS Registry Number.

1133982-01-0Upstream product

1133982-01-0Downstream Products

1133981-93-7 4O-tert-butyldimethylsilyl-3-O-carbamoyl-6-O-p-toluenesulfonyl-D-glucal

1133982-01-0Relevant academic research and scientific papers

Protecting group and solvent control of stereo-and chemoselectivity in glucal 3-carbamate amidoglycosylation

Gupta, Ritu,Sogi, Kimberly M.,Bernard, Sarah E.,Decatur, John D.,Rojas, Christian M.

supporting information; experimental part, p. 1527 - 1530 (2009/09/06)

In the Rh2(OAc)4-catalyzed amidoglycosylation of glucal 3-carbamates, anomeric stereoselectivity and the extent of competing C3-H oxidation depend on the 4O and 6O protecting groups. Acyclic protection permits high α-anomer selectivi

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