추천 제품
양식
liquid
Quality Level
농도
1.0 M in heptane
bp
44-46 °C
density
0.724 g/mL at 25 °C
SMILES string
C[Zn]C
InChI
1S/2CH3.Zn/h2*1H3;
InChI key
AXAZMDOAUQTMOW-UHFFFAOYSA-N
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일반 설명
Dimethylzinc (Zn(CH3)2) is a methylating reagent used to prepare methylated organic compounds as well as organometallic compounds containing methyl groups . It is also utilized as a reagent to prepare amino alcohols, oximes, and hydrazones from arylamines, alkoxyamines, and dialkylhydrazines respectively, by radical addition reaction in the presence of air and THF.
Dimethylzinc is a diorganozinc reagent and nucleophile used in the synthesis of propargylic amines.
Dimethylzinc is a diorganozinc reagent and nucleophile used in the synthesis of propargylic amines.
애플리케이션
Dimethylzinc solution can be used as:
- A catalyst with nickel for the stereoselective C−2 alkenylation and dialkenylation of pyridine derivatives by alkynes to give monoalkenylation products.
- A reagent with aldehydes and 2-methoxyaniline for the synthesis of enantioselective alkyl and aralkyl secondary amines via one-pot three-component coupling reaction in the presence of zirconium tetraisopropoxide.
- A methylating reagent for methylation of fluoroalkylated pyruvates in the presence of copper/chiral diphosphine catalyst.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Skin Corr. 1B - STOT SE 3 - Water-react 2
표적 기관
Central nervous system
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 3
Flash Point (°F)
30.2 °F - closed cup
Flash Point (°C)
-1 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles
이미 열람한 고객
Beilstein journal of organic chemistry, 14, 576-582 (2018-04-07)
The catalytic asymmetric methylation of fluoroalkylated pyruvates is shown with dimethylzinc as a methylating reagent in the presence of a copper catalyst bearing a chiral phosphine ligand. This is the first catalytic asymmetric methylation to synthesize various α-fluoroalkylated tertiary alcohols
Formation of transient dimethylzinc, dimethylcadmium, and dimethyllead species via methylation of zinc (2+), cadmium (2+), and lead (2+) by a trans-dimethylcobalt complex
Inorganic Chemistry, 16(10), 2512-2515 (1977)
Dimethylzinc-mediated alkynylation of imines
The Journal of Organic Chemistry, 71, 1558-1562 (2006)
Accounts of chemical research, 42(2), 345-355 (2008-12-31)
Developments in modern organic synthesis owe much to the field of radical chemistry. Mild reaction conditions, high selectivity, good functional group tolerance and high product yield are features that have made reactions involving radical species indispensable tools for synthetic chemists.
Diethylzinc
Synlett, 1937-1938 (2014)
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