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Benzene, 1-methyl-4-[3-(2-propenyloxy)-1-propynyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

862972-84-7

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862972-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862972-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,9,7 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 862972-84:
(8*8)+(7*6)+(6*2)+(5*9)+(4*7)+(3*2)+(2*8)+(1*4)=217
217 % 10 = 7
So 862972-84-7 is a valid CAS Registry Number.

862972-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-4-(3-prop-2-enoxyprop-1-ynyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1-methyl-4-[3-(2-propenyloxy)-1-propynyl]

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:862972-84-7 SDS

862972-84-7Relevant academic research and scientific papers

Atom-Economical Ni-Catalyzed Diborylative Cyclization of Enynes: Preparation of Unsymmetrical Diboronates

Cabrera-Lobera, Natalia,Quirós, M. Teresa,Brennessel, William W.,Neidig, Michael L.,Bu?uel, Elena,Cárdenas, Diego J.

, p. 6552 - 6556 (2019/08/20)

We report a Ni-catalyzed diborylative cyclization of enynes that affords carbo- and heterocycles containing both alkyl- and alkenylboronates. The reaction is fully atom-economical, shows a broad scope, and employs a powerful and inexpensive catalytic Ni-b

Iron-Catalyzed Hydroborylative Cyclization of 1,6-Enynes

Cabrera-Lobera, Natalia,Rodríguez-Salamanca, Patricia,Nieto-Carmona, Juan C.,Bu?uel, Elena,Cárdenas, Diego J.

, p. 784 - 788 (2017/11/29)

We report first Fe-catalyzed hydroborylative cyclization reaction. The process provides one C?C and one C?B bond in a single operation and shows a wide scope, allowing the formation of carbo- and heterocycles containing a homoallylic boryl unit that can b

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

Formate as a CO surrogate for cascade processes: Rh-catalyzed cooperative decarbonylation and asymmetric Pauson-Khand-type cyclization reactions

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

, p. 2633 - 2635 (2008/02/08)

A rhodium-(S)-xyl-BINAP complex-catalyzed tandem formate decarbonylation and [2 + 2 + 1] carbonylative cyclization is described; this cooperative process utilizes formate as a condensed CO source, and the newly developed cascade protocol can be extended t

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

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