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15833-75-7

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15833-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15833-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,3 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15833-75:
(7*1)+(6*5)+(5*8)+(4*3)+(3*3)+(2*7)+(1*5)=117
117 % 10 = 7
So 15833-75-7 is a valid CAS Registry Number.

15833-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyloxolane

1.2 Other means of identification

Product number -
Other names 3.3-Dimethyl-tetrahydrofuran

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:15833-75-7 SDS

15833-75-7Relevant articles and documents

Toward Orally Absorbed Prodrugs of the Antibiotic Aztreonam. Design of Novel Prodrugs of Sulfate Containing Drugs. Part 2

Ding, Pingyu,Duncton, Matthew A. J.,Fan, Dazhong,Gordon, Eric M.,Grygorash, Ruslan,Li, Xianfeng,Low, Eddy,Ni, Zhi-Jie,Qi, Longwu,Sun, Jiawei,Wang, Brian J.,Yu, Guijun

supporting information, p. 162 - 165 (2020/01/31)

Aztreonam, first discovered in 1980, is an FDA approved, intravenous, monocyclic beta-lactam antibiotic. Aztreonam is active against Gram-negative bacteria and is still used today. The oral bioavailability of aztreonam in humans is less than 1%. Herein we describe the design and synthesis of potential oral prodrugs of aztreonam.

Chemical Activation Study of the Reactions of Methylene with Oxetan and 3,3-Dimethyloxetan

Frey, Henry M.,Pidgeon, Ivy M.

, p. 1237 - 1248 (2007/10/02)

Methylene (singlet) formed by the photolysis of ketene (313 nm) reacts with oxetan to yield 2-methyl- and 3-methyloxetans by insertion in the C-H bonds and probably also tetrahydrofuran.These products are formed chemically activated and undergo unimolecular decomposition unless collisionally stabilized.Using perfluoropropane as the bath gas, the results obtained with 2-methyloxetan have been interpreted using RRKM theory and a step-ladder model with a most probable step size of ca. 9 kJ mol-1.Using 206 nm radiation yields methylene with excess energy, some of which is still present when it reacts, and results in the production of 2-methyloxetan with an average lifetime approximately one-half that of the energised molecule produced when 313 nm radiation is used.Similarly methylene reacts with 3,3-dimethyloxetan to yield chemically activated 3-ethyl-3-methyloxetan and 2,3,3-trimethyloxetan.A third compound tentatively identified as 3,3-dimethyltetrahydrofuran is also formed.The decomposition of these 3 molecules has been followed and in the case of the ethylmethyloxetan the average energy transferred in collision with 3,3-dimethyloxetan has been found to be ca. 6.5 kJ mol-1.Some deductions can be made about the Arrhenius parameters for the thermal decomposition of the (as yet unreported) trimethyloxetan and the dimethyltetrahydrofuran.

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