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3,4-dihydro-1H-5,2,1-benzoxathiazepine 2,2-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90220-51-2

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90220-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90220-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,2 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90220-51:
(7*9)+(6*0)+(5*2)+(4*2)+(3*0)+(2*5)+(1*1)=92
92 % 10 = 2
So 90220-51-2 is a valid CAS Registry Number.

90220-51-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydro-1H-5,2λ<sup>6</sup>,1-benzoxathiazepine 2,2-dioxide

1.2 Other means of identification

Product number -
Other names 3,4-dihydro-1H-5,2

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90220-51-2 SDS

90220-51-2Downstream Products

90220-51-2Relevant academic research and scientific papers

Solution and Flash Vacuum Pyrolyses of 3-Arylpropanesulfonyl and 2-(Aryloxy)ethanesulfonyl Azides. Synthesis of 7-Membered Sultams

Abramovitch, Rudolph A.,Kress, Albert O.,McManus, Samuel P.,Smith, Maurice R.

, p. 3114 - 3121 (2007/10/02)

The solution and flash vacuum pyrolyses of 3-arylpropanesulfonyl azides have been studied and the results compared with those of the corresponding 2-arylethanesulfonyl azides.The best yields of 7-membered ring sultams are formed on solution decomposition in Freon 113.Hydrogen abstraction and solvent insertion products are obtained mainly in hydrocarbon solvents.The structure of the 7-membered sultams have been established unambiguously and an authentic sample of the parent 2,3,4,5-tetrahydro-1,2-thiazepine 1,1-dioxide prepared.Decomposition of 3-(2,6-dichlorophenyl)propanesulfonyl azide (22) leads to a 6,9-dichloro sultam (33c) via a 1,2-chlorine shift.FVP of 3-(2-mesityl)propanesulfonyl azide (20) gave a good yield of the 7-membered ring sultam (34)(1,2-methyl shift).FVP of 3-phenyl-1-propanesulfonyl azide (16) at 995 deg C (0.05 mm) gave, among other products, a 6.2percent yield of 5,6,7,8-tetrahydroquinoline (39).The formation of these products is discussed.Thermolysis of 2-(aryloxy)ethanesulfonyl azides gave the corresponding 7-membered ring sultams 27 as well.

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