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1-(Ethylsulfanyl)buta-1,3-diyne is an organic compound characterized by its unique structure, which includes a buta-1,3-diyne backbone with an ethylsulfanyl group attached to the first carbon atom. This molecule is composed of a carbon-carbon triple bond at both ends of the buta-1,3-diyne chain, with the ethylsulfanyl group (-CH2CH3-S-) providing a sulfur-containing functional group. The compound is known for its potential applications in the synthesis of various organic compounds and materials, particularly in the fields of pharmaceuticals and specialty chemicals. Its chemical formula is C6H8S, and it has a molecular weight of 112.20 g/mol. The presence of the triple bonds and the sulfur atom in the molecule contribute to its reactivity and unique chemical properties, making it a valuable intermediate in organic synthesis.

1609-42-3

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1609-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1609-42:
(6*1)+(5*6)+(4*0)+(3*9)+(2*4)+(1*2)=73
73 % 10 = 3
So 1609-42-3 is a valid CAS Registry Number.

1609-42-3SDS

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-ethylsulfanylbuta-1,3-diyne

1.2 Other means of identification

Product number -
Other names 1-(ethylsulfanyl)buta-1,3-diyne

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:1609-42-3 SDS

1609-42-3Relevant academic research and scientific papers

A stereoselective synthesis of 1-phenyl-1-buten-3-yne and some 1-heteroaryl analogues

Fossatelli, Marco,Van Der Kerk, Anca C. T. H. M.,Vasilevsky, Sergei F.,Brandsma, Lambert

, p. 4229 - 4232 (2007/10/02)

Z-Enynes, RCH=CHC≡CH (R= phenyl, 2-furyl, 2- and 3-thienyl and 3-pyridyl) can be obtained in ~ 40% overall yields and with a stereoselectivity of> 95% by Pd/Cu-catalyzed cross-coupling of the readily available enyne sulfide HC≡CCH=CHSC2H5

An efficient synthetic method for 1-N,N-dialkylamino-1,3-pentadiynes

Brandsma,Walda,Oosterveld

, p. 73 - 77 (2007/10/02)

The diyne amines CH3C≡CC≡CNR2 (R = CH3 or C2H5) have been synthesized with greater than 50% overall yields starting from 1,4-dichloro-2-butyne, the last step being a base-catalyzed isomerization of HC≡CC≡CCH2NR2.

Investigation in the field of biacetylene derivatives. XXXIX. A new method for the production of alkylthioenynyl alcohols and their transformations with participation of the hydroxyl group

Volkova, K. A.,Levanova, E. P.,Nikol'skaya, A. N.,Volkov, A. N.,Trofimov, B. A.

, p. 1187 - 1191 (2007/10/02)

A simple and effective method was developed for the production of tertiary alkylthioenynyl alcohols from biacetylene, ketones, and thiols in liquid ammonia.A series of their derivatives involving participation of the hydroxyl group were obtained (β-cyanoethyl, trimethylsilyl, and glycidyl ethers and esters, acetals).

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