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5,5-diMethyl-3-hexyn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105418-43-7

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105418-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105418-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,1 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105418-43:
(8*1)+(7*0)+(6*5)+(5*4)+(4*1)+(3*8)+(2*4)+(1*3)=97
97 % 10 = 7
So 105418-43-7 is a valid CAS Registry Number.

105418-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethylhex-3-yn-1-ol

1.2 Other means of identification

Product number -
Other names 3-Hexyn-1-ol,5,5-dimethyl

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:105418-43-7 SDS

105418-43-7Relevant articles and documents

Development of an Alkyne Analogue of the de Mayo Reaction: Synthesis of Medium-Sized Carbacycles and Cyclohepta[b]indoles

Tymann, David,Tymann, Dina Christina,Bednarzick, Ulf,Iovkova-Berends, Ljuba,Rehbein, Julia,Hiersemann, Martin

supporting information, p. 15553 - 15557 (2018/11/10)

Embedded medium-sized carbacycles and cyclohepta[b]indoles occur frequently as scaffold elements in natural products and bioactive compounds. Described herein is a conceptionally novel photochemically triggered cascade process to these scaffolds. Key to the cascading ring-expansion process is an unprecedented intramolecular alkyne analogue of the de Mayo reaction.

Synthesis and Structure-Activity Relationships of the Novel Homopropargylamine Antimycotics

Nussbaumer, Peter,Leitner, Ingrid,Stuetz, Anton

, p. 610 - 615 (2007/10/02)

Analogues of the antimycotic allylamine terbinafine were prepared in which the naphthalene and the tert-butylacetylene moieties were preserved, but the spacer between these two groups was varied, and the antifungal activity of the new compounds was evalua

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