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19781-24-9

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19781-24-9 Usage

Description

3,3-DIMETHYL-2-PENTANOL is an organic compound with the molecular formula C7H16O. It is a colorless liquid with a distinctive odor and is commonly used as an intermediate in the synthesis of various chemicals.

Uses

Used in Chemical Synthesis:
3,3-DIMETHYL-2-PENTANOL is used as an intermediate in the synthesis of 3,3-Dimethyl-1-pentene (D476815), which is an important compound in the chemical industry. It serves as a key building block for the production of various chemicals and materials.
Used in Analytical Chemistry:
3,3-DIMETHYL-2-PENTANOL is also used to estimate the gas chromatography retention of other compounds. This application is crucial in the field of analytical chemistry, as it helps in the identification and quantification of different substances in a mixture.

Check Digit Verification of cas no

The CAS Registry Mumber 19781-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19781-24:
(7*1)+(6*9)+(5*7)+(4*8)+(3*1)+(2*2)+(1*4)=139
139 % 10 = 9
So 19781-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O/c1-5-7(3,4)6(2)8/h6,8H,5H2,1-4H3

19781-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethylpentan-2-ol

1.2 Other means of identification

Product number -
Other names Methyl-tert.-amyl-carbinol

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:19781-24-9 SDS

19781-24-9Relevant articles and documents

Slaugh et al.

, p. 3180 (1963)

Catalytic and asymmetric [2,3]sigmatropic rearrangement: Co(III)-salen catalyzed S-ylide formation from allyl aryl sulfides and their rearrangement

Fukuda, Tsutomu,Irie, Ryo,Katsuki, Tsutomu

, p. 649 - 664 (2007/10/03)

Reaction of allyl aryl sulfides and α-diazoacetic acid esters in the presence of optically active Co(III)-salen complex (8-Br) provided 3- substituted 2-arylthio-4-pentenoic acid esters stereoselectively by way of enantioselective S-ylide formation and subsequent diastereoselective [2,3]sigmatropic rearrangement. For example, the reaction of cinnamyl phenyl sulfide and (-)-menthyl α-diazoacetate provided (-)-menthyl (2R,3S)-2- phenylthio-3-phenyl-4-pentenoate of 74% de preferentially.

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