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Benzene, 4-(1-butenyl)-1,2-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68719-73-3

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68719-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68719-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,1 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68719-73:
(7*6)+(6*8)+(5*7)+(4*1)+(3*9)+(2*7)+(1*3)=173
173 % 10 = 3
So 68719-73-3 is a valid CAS Registry Number.

68719-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-but-1-enyl-1,2-dimethoxybenzene

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:68719-73-3 SDS

68719-73-3Downstream Products

68719-73-3Relevant academic research and scientific papers

PHENYLBUTANOIDS FROM ZINGIBER CASSUMUNAR

Tuntiwachwuttikul, Pittaya,Pancharoen, Orasa,Jaipetch, Thaworn,Reutrakul, Vichai

, p. 1164 - 1165 (1981)

Five novel phenylbutanoids have been isolated from the rhizomes of Zingiber cassumunar. 3,4-Dimethoxybenzaldehyde and 2,4,5-trimethoxy-benzaldehyde are also reported from the same source.Key Word Index- Zingiber cassumunar; structure elucidation and syntheses; 1-arylbut-1,3-dienes; 1-arylbut-1-enes; (E)-4-(3',4'-dimethoxy)but-3-en-1-yl palmitate; aryl aldehydes.

Oxocarbons and related compounds. 27. Synthesis of dihydrocyclobuta[a]naphthalene-1,2-diones and cyclobuta[a]naphthalene-1,2-diones via annulation of alkoxy-(1-alkenyl)benzenes with 3-chloro-3-cyclobutene-1,2-dione. Scope and limitations

Schmidt, Arthur H.,Kircher, Gunnar,Spring, Mathias,Hendriok, Markus W.,Kuenz, Christian

, p. 564 - 574 (2007/10/03)

The reaction of alkoxy-(1-alkenyl)benzenes with semisquaric chloride (3) has been investigated systematically. 1,2-Dialkoxy- and 1-alkoxy′-2-alkoxy″-4-(1-alkenyl)benzenes (6a-j) and (11a-i) react with 3 to give the 3,4-dihydrocyclobuta[a]naphthalene-1,2-diones(8a-j) and (12a-i). Treatment of the dihydrocyclobuta[a]naphthalene-1,2-diones with 1.2 equiv. bromine effects dehydrogenation and affords cyclobuta[a]naphthalene-1,2-diones(9a-e) and (13b-f). Any efforts to extend this annulation reaction to dimethoxy-(1-alkenyl)benzenes with the methoxy groups in other than the 1,2-positions, e. g. 14a, b, 16a, b have been unsuccessful. The reaction of 1,2,3-trimethoxy-4-(1-propenyl) [and 4-(1-butenyl)]-benzenes (18a) and (18b) with semisquaric chloride (3) leads to the elimination of HCl and CH3OH and gives 5,6-dimethoxy-3-methyl [and 3-ethyl]-cyclobuta[a]naphthalene-1,2-diones (20a) and (20b). The reaction pathway of this novel annulation reaction is discussed.

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