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5349-02-0

4,4-dimethyl-3,5,10,11-tetraoxatricyclo[6.2.1.0~2,6~]undec-7-yl 4-methylbenzenesulfonate, also known as a chemical compound, is a complex organic molecule with a unique structure. It consists of a tricyclo[6.2.1.0~2,6~]undecane ring system with a 4,4-dimethyl group, a 3,5,10,11-tetraoxa group, and a 4-methylbenzenesulfonate group attached to it. 4,4-dimethyl-3,5,10,11-tetraoxatricyclo[6.2.1.0~2,6~]undec-7-yl 4-methylbenzenesulfonate (non-preferred name) is characterized by its specific arrangement of atoms and functional groups, which contribute to its distinct chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. Due to its complexity, it is essential to understand its structure and properties to harness its potential in a safe and effective manner.

5349-02-0

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5349-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5349-02-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5349-02:
(6*5)+(5*3)+(4*4)+(3*9)+(2*0)+(1*2)=90
90 % 10 = 0
So 5349-02-0 is a valid CAS Registry Number.

5349-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-ANHYDRO-2,3-O-ISOPROPYLIDENE-.β.-D-MANNOPYRANOSE, P-TOLUENESULFONATE

1.2 Other means of identification

Product number -
Other names O2,O3-isopropylidene-D-threo-4,5-dideoxy-pent-4-enose

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:5349-02-0 SDS

5349-02-0Relevant articles and documents

Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-d-hexopyranoses with diethylaminosulphur trifluoride

Karban, Jindrich,Cisarova, Ivana,Strasak, Tomas,Sastna, Lucie Cervenkova,Sykora, Jan

supporting information; scheme or table, p. 394 - 403 (2012/02/05)

A complete series of eight 1,6:2,3- and 1,6:3,4-dianhydro-β-d- hexopyranoses were subjected to fluorination with DAST. The 1,6:3,4- dianhydropyranoses yielded solely products of skeletal rearrangement resulting from migration of the tetrahydropyran oxygen

Synthesis and enzyme-inhibitory activity of methyl acarviosin analogues having the α-manno configuration

Ogawa, Seiichiro,Nakamura, Yoshikazu

, p. 79 - 90 (2007/10/02)

Two methyl acarviosin analogues 3a and 4a, having the α-manno configuration, and their dihydro derivatives 6a and 7a were synthesized by coupling the protected pseudo-sugar epoxides with methyl 4-amino-4-deoxy- and -4,6-dideoxy-α-D-mannopyranoside.Similar

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