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N-(3-phenylprop-2-yn-1-yl)prop-2-en-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98729-78-3

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98729-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98729-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,2 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98729-78:
(7*9)+(6*8)+(5*7)+(4*2)+(3*9)+(2*7)+(1*8)=203
203 % 10 = 3
So 98729-78-3 is a valid CAS Registry Number.

98729-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-N-prop-2-enylprop-2-yn-1-amine

1.2 Other means of identification

Product number -
Other names -

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:98729-78-3 SDS

98729-78-3Relevant academic research and scientific papers

Microwave-assisted rhodium-complex-catalyzed cascade decarbonylation and asymmetric Pauson-Khand-type cyclizations

Hang, Wai Lee,Lai, Na Lee,Chan, Albert S. C.,Fuk, Yee Kwong

supporting information; experimental part, p. 3403 - 3406 (2009/04/07)

Microwave-assisted Rh-diphosphane-complex-catalyzed dual catalysis is reported. This cooperative process provides [2+2+1] cycloadducts by sequential decarbonylation of aldehyde or formate and carbonylation of enynes within a short period of time. Various

Iridium-catalyzed cascade decarbonylation/highly enantioselective Pauson-Khand-type cyclization reactions

Kwong, Fuk Yee,Lee, Hang Wai,Lam, Wai Har,Qiu, Liqin,Chan, Albert S.C.

, p. 1238 - 1252 (2007/10/03)

An easily accessible chiral iridium-BINAP complex can effect the cooperative processes of decarbonylation of an aldehyde and cascaded enantioselective Pauson-Khand-type reaction. A survey of ligands revealed that atropisomeric aryl-diphosphine ligands wer

Rhodium-bisbenzodioxanphos complex-catalyzed homogeneous enantioselective Pauson-Khand-type cyclization in alcoholic solvents

Fuk, Yee Kwong,Hang, Wai Lee,Qiu, Liqin,Wai, Har Lam,Li, Yue-Ming,Hoi, Lun Kwong,Chan, Albert S. C.

, p. 1750 - 1754 (2007/10/03)

The chiral atropisomeric diphosphane ligand (S)-BisbenzodioxanPhos was found to be highly effective in the co-operative processeses of aldehyde decarbonylation and cascaded enantioselective Pauson-Khand-type reactions. Various 1,6-enynes were transformed

Rhodium-catalyzed asymmetric aqueous Pauson-Khand-type reaction

Kwong, Fuk Yee,Li, Yue Ming,Lam, Wai Har,Qiu, Liqin,Lee, Hang Wai,Yeung, Chi Hung,Chan, Kin Shing,Chan, Albert S. C.

, p. 3872 - 3880 (2007/10/03)

An interesting rhodium-catalyzed asymmetric aqueous Pauson-Khand-type reaction was developed. A chiral atropisomeric dipyridyldiphosphane ligand was found to be highly effective in this system. This operationally simple protocol allows both catalyst and r

The rhodium-catalyzed Pauson-Khand reaction

Kobayashi, Toshitake,Koga, Yuji,Narasaka, Koichi

, p. 73 - 87 (2007/10/03)

A rhodium carbonyl complex, [RhCl(CO)2]2, serves as a catalyst of the intra- and inter-molecular Pauson-Khand reaction. By the use of the rhodium catalyst, cyclopentenone derivatives are prepared from various 1,6- and 1,7-enynes unde

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