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"Benzene, (2,3-dimethyl-3-butenyl)-" is an organic compound with the chemical formula C12H16. It is a derivative of benzene, where a 2,3-dimethyl-3-butenyl group is attached to the benzene ring. Benzene, (2,3-dimethyl-3-butenyl)- is also known as 2,3-dimethyl-3-butenylbenzene or alpha-methylstyrene. It is a colorless liquid with a strong, pungent odor and is insoluble in water. The compound is used as a chemical intermediate in the synthesis of various organic compounds, such as polymers and pharmaceuticals. Due to its reactive nature, it is important to handle Benzene, (2,3-dimethyl-3-butenyl)- with care, as it may pose health risks and environmental concerns.

6700-98-7

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6700-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6700-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6700-98:
(6*6)+(5*7)+(4*0)+(3*0)+(2*9)+(1*8)=97
97 % 10 = 7
So 6700-98-7 is a valid CAS Registry Number.

6700-98-7Downstream Products

6700-98-7Relevant academic research and scientific papers

Regio- and Stero-selective Desulphurizative γ-Substitution of α-Substituted β-Methylallyl Sulphoxides and Sulphones with Lithium Dialkylcuprates providing Trisubstituted Olefins

Masaki, Yukio,Sakuma, Kazuhiko,Kaji, Kenji

, p. 1170 - 1176 (2007/10/02)

α-Substituted β-methylallyl sulphoxides (2) and sulphones (3) undergo regio- and stereo-selective desulphurizative γ-substitution by the action of lithium dialkylcuprates in ether.The reaction provides a new method for the synthesis of trisubstituted E-ol

COMPLEXES OF TRANSITION METALS IN THE CHEMISTRY OF CONJUGATED SYSTEMS. III. REACTION OF DIENE HYDROCARBONS WITH ORGANOMAGNESIUM COMPOUNDS IN THE PRESENCE OF SALTS AND COMPLEXES OF TRANSITION METALS

Zubritskii, L. M.,Romashchenkova, N. D.,Petrov, A. A.

, p. 2157 - 2167 (2007/10/02)

The effect of the structure of the reagents and the nature of the catalyst on the direction and selectivity in the reaction of 1,3-dienes and their derivatives with aromatic Grignard reagents was investigated.It was shown that in the presence of salts and complexes of iron(III) 1,3-alkadienes R1CH=C(R2)C(R3)=CH2 react with arylmagnesium halides to form trans-(E)-1-aryl-1,3-alkadienes, whereas the sterically hindered (R2, R3=CH3) cyclic 1,3-alkadienes and also 1,2-alkadienes give mainly adducts (1:1).Catalysis by the phosphine complexes of nickel(II) leads to the formation of telomeric (2:1) (E)-1-aryl-2,7- and (E,E)-1-aryl-2,6-alkadienes.The results demonstrate the determining role of the stereochemical conditions for the coordination of the diene in the course of the reaction and also the significant contribution from the processes of one-electron reduction of the catalyst.

Regio- and Stereo-selective γ-Substitution of Allylic Sulphoxides and Sulphones with Lithium Dialkylcuprates. A New Synthesis of Trisubstituted Olefins

Masaki, Yukio,Sakuma, Kazuhiko,Kaji, Kenji

, p. 434 - 435 (2007/10/02)

A new regio- and stereo-selective γ-substitution of allylic sulphoxides and sulphones with lithium dialkylcuprates providing a promising new method for the preparation of trisubstituted olefins in particular is described.

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