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19549-98-5

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19549-98-5 Usage

General Description

3,6-Dimethyl-1-heptyn-3-ol is a synthetic organic compound that is colorless and typically exists in liquid form. It belongs to the group of aliphatic acyclic compounds, specifically those that are alkynes. 3,6-DIMETHYL-1-HEPTYN-3-OL may be used as an intermediate in organic synthesis for the production of other chemicals. It is important to note that the chemical can cause irritation upon skin contact or if inhaled, thus safety measures should be undertaken while handling it. However, specific applications and uses of this particular chemical are not widely documented in scientific literature.

Check Digit Verification of cas no

The CAS Registry Mumber 19549-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,4 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19549-98:
(7*1)+(6*9)+(5*5)+(4*4)+(3*9)+(2*9)+(1*8)=155
155 % 10 = 5
So 19549-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-5-9(4,10)7-6-8(2)3/h1,8,10H,6-7H2,2-4H3/t9-/m0/s1

19549-98-5 Well-known Company Product Price

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  • TCI America

  • (D1266)  3,6-Dimethyl-1-heptyn-3-ol  >98.0%(GC)

  • 19549-98-5

  • 5mL

  • 1,450.00CNY

  • Detail

19549-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dimethylhept-1-yn-3-ol

1.2 Other means of identification

Product number -
Other names 3,6-dimethyl-1-heptyne-3-ol

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:19549-98-5 SDS

19549-98-5Relevant articles and documents

Regioselective Vinylation of Remote Unactivated C(sp3)?H Bonds: Access to Complex Fluoroalkylated Alkenes

Wu, Shuo,Wu, Xinxin,Wang, Dongping,Zhu, Chen

supporting information, p. 1499 - 1503 (2019/01/04)

Regioselective incorporation of a particular functional group into aliphatic sites by direct activation of unreactive C?H bonds is of great synthetic value. Despite advances in radical-mediated functionalization of C(sp3)?H bonds by a hydrogen-atom transfer process, the site-selective vinylation of remote C(sp3)?H bonds still remains underexplored. Reported herein is a new protocol for the regioselective vinylation of unactivated C(sp3)?H bonds. The remote C(sp3)?H activation is promoted by a C-centered radical instead of the commonly used N and O radicals. The reaction possesses high product diversity and synthetic efficiency, furnishing a plethora of synthetically valuable E alkenes bearing tri-/di-/mono-fluoromethyl and perfluoroalkyl groups.

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