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1-Dodecen-3-yne. is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74744-36-8

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74744-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74744-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,4 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74744-36:
(7*7)+(6*4)+(5*7)+(4*4)+(3*4)+(2*3)+(1*6)=148
148 % 10 = 8
So 74744-36-8 is a valid CAS Registry Number.

74744-36-8SDS

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 dodec-1-en-3-yne

1.2 Other means of identification

Product number -
Other names 1-dodecene-3-yne

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:74744-36-8 SDS

74744-36-8Relevant academic research and scientific papers

Cobalt-catalyzed cross-coupling of alkynyl Grignard reagents with alkenyl triflates

Shirakawa, Eiji,Sato, Takahiro,Imazaki, Yusuke,Kimura, Takahiro,Hayashi, Tamio

, p. 4513 - 4515 (2007)

Alkenyl triflates in combination with Co(acac)3 as a catalyst were found to be excellent coupling partners of alkynyl Grignard reagents, where no special additives (even a phosphine ligand) but a common solvent, THF, are required to obtain vari

Triple-Bond Insertion Triggers Highly Regioselective 1,4-Aminomethylamination of 1,3-Enynes with Aminals Enabled by Pd-Catalyzed C-N Bond Activation

Zhang, Yanchen,Yu, Bangkui,Gao, Binjian,Zhang, Tianze,Huang, Hanmin

supporting information, (2019/01/21)

A highly chemo- and regioselective 1,4-aminomethylamination of simple enynes with aminals to allenic 1,5-diamines by taking advantage of C-N bond activation has been reported. The reaction proceeds under mild reaction conditions and can be performed under

Triple-Bond Insertion Triggers Highly Regioselective 1,4-Aminomethylamination of 1,3-Enynes with Aminals Enabled by Pd-Catalyzed C-N Bond Activation

Zhang, Yanchen,Yu, Bangkui,Gao, Binjian,Zhang, Tianze,Huang, Hanmin

supporting information, p. 535 - 539 (2019/01/24)

A highly chemo- and regioselective 1,4-aminomethylamination of simple enynes with aminals to allenic 1,5-diamines by taking advantage of C-N bond activation has been reported. The reaction proceeds under mild reaction conditions and can be performed under

Silaborations of 1,3-enynes - Substrate controlled allene/1,3-diene selectivity

Lueken, Christian,Moberg, Christina

supporting information; experimental part, p. 2505 - 2508 (2009/05/26)

(Chemical Equation Presented) Silaboration of 1,3-enynes catalyzed by group 10 metal complexes affords 1,3-dienes with vinylborane and vinylsilane functions or 1,2-dienes with allylborane and vinylsilane functions. The type of product formed is determined

Insertion of 1-chloro-1-lithioalkenes into organozirconocenes. A versatile synthesis of stereodefined unsaturated systems

Kasatkin, Aleksandr,Whitby, Richard J.

, p. 7039 - 7049 (2007/10/03)

Hydrozirconation of alkenes and alkynes, followed by insertion of 1- halo-1-lithio-1-alkenes, generated in situ by lithium tetramethylpiperidide deprotonation of vinyl halides, affords vinylzirconocene species which may be further elaborated. The method provides easy access to many structures including terminal (3E)- and (3Z)-1,3-dienes and (3E,5E)- and (3Z,5E)-1,3,5- trienes, and internal (E,Z)-dienes,(E,Z,E)-trienes, and (1E, 3Z)1,3-dien-5- ynes. Insertion of 2-monosubstituted 1-halo-1-lithio-1-alkenes occurs with clean inversion of configuration of the sp2-carbenoid carbon. Carbenoids derived by deprotonation of 2,2-disubstituted 1-halo-1-alkenes gave poor stereocontrol probably due to isomerization before insertion into the organozirconium species. Insertion of vinyl carbenoids into alkynylzirconocenes affords terminal (3E)- or (3Z)-1,3-dien-5-ynes, internal (1E,3Z)-1,3-dien-5-ynes, and (Z)-3-en-1,5-diynes.

Control of the Propargylic Radical Stabilization by Carbon-Chain Length in Manganese(III)-Mediated Reactions of 1-Alken-3-ynes. - A Facile Synthetic Way to Long-Chain 4-Acetoxy-5-alkynoic Acids

Melikyan, Gagik G.,Mkrtchyan, Varsik M.,Badanyan, Shaliko O.,Vostrowsky, Otto,Bestmann, Hans Juergen

, p. 2037 - 2040 (2007/10/02)

By investigation of reactions of 1-alken-3-ynes RCC-CH=CH2 4 with acetic acid/ acetic anhydride, mediated by manganese(III) acetate, it has been found that the stabilization of propargylic radical adducts depends on the carbon-chain length of R in 4.R=C8H17 is shown to be the "critical" chain length when ligand transfer reaction appears to be the only way of stabilization of intermediates, thus providing a facile one-step access to long-chain 4-acetoxy-5-alkynoic caids.The dependence of the product ratios on the AcOH/Ac2O ratio has also been demonstrated. Key Words: 1-Alken-3-ynes / Manganese(III) acetate / Propargyl radical / Ligand-transfer reaction / Electron-transfer reaction

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