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4-(METHYLTHIO)PHENYLZINC IODIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

307496-24-8

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307496-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 307496-24-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,4,9 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 307496-24:
(8*3)+(7*0)+(6*7)+(5*4)+(4*9)+(3*6)+(2*2)+(1*4)=148
148 % 10 = 8
So 307496-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7S.HI.Zn/c1-8-7-5-3-2-4-6-7;;/h3-6H,1H3;1H;/q;;+1/p-1/rC7H7ISZn/c1-9-6-2-4-7(10-8)5-3-6/h2-5H,1H3

307496-24-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H58137)  4-(Methylthio)phenylzinc iodide, 0.5M in THF, packaged under Argon in resealable ChemSeal? bottles   

  • 307496-24-8

  • 50ml

  • 3030.0CNY

  • Detail

307496-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(METHYLTHIO)PHENYLZINC IODIDE

1.2 Other means of identification

Product number -
Other names 4-(Methylthio)phenylzinc iodide,0.5M in THF,packaged under Argon in resealable CheMSeal^t bottles

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:307496-24-8 SDS

307496-24-8Downstream Products

307496-24-8Relevant academic research and scientific papers

Sequential Organozinc Formation and Negishi Cross-Coupling of Amides Catalysed by Cobalt Salt

Dorval, Céline,Dubois, Elodie,Bourne-Branchu, Yann,Gosmini, Corinne,Danoun, Grégory

supporting information, p. 1777 - 1780 (2019/02/26)

Herein, a cobalt-catalysed Negishi-type cross-coupling of amide derivatives is described. Apart from being the first example of cobalt-catalysed Negishi-type coupling of amides, the process described employs a unique, simple, and cheap catalytic system to perform both the organozinc formation and the Negishi-type coupling. Indeed, the same cobalt(II) bromide salt used to form the arylzinc species from aryl bromides is then re-used to perform the cross coupling of this resulting arylzinc with N-benzoyl glutarimides at room temperature. The main advantages of the reaction presented are its robustness and ease of use. Indeed, the reactions of organozinc formation and Negishi-type coupling are performed without precautions toward water or oxygen. (Figure presented.).

Cobalt-catalyzed electrophilic amination of arylzincs with N-chloroamines

Qian, Xin,Yu, Zailu,Auffrant, Audrey,Gosmini, Corinne

supporting information, p. 6225 - 6229 (2013/07/05)

Roles reversed: An efficient cobalt-catalyzed electrophilic amination of arylzinc reagents has been achieved. A variety of functionalized arylzincs and N-chloroamines were coupled under mild conditions (see scheme). Both secondary and tertiary arylamines were obtained in moderate to excellent yields. Copyright

Cobalt-catalysed synthesis of highly substituted styrene derivatives via arylzincation of alkynes

Corpet, Martin,Gosmini, Corinne

supporting information, p. 11561 - 11563,3 (2012/12/12)

A new two-step procedure was developed by carbozincation of internal and terminal alkynes to synthesise highly functionalised vinylzinc bromides. Various tri and tetrasubstituted alkenes were prepared in moderate to good yields under mild reaction conditions in a stereo-selective manner. This methodology represents an interesting alternative to previously known methods. This journal is

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