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1H-Benz[g]indole-2,3,3a,4,7,8(9H)-hexacarboxylic acid, 6,9b-dihydro-1-(phenylmethyl)-, hexamethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144425-41-2

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144425-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144425-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,2 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 144425-41:
(8*1)+(7*4)+(6*4)+(5*4)+(4*2)+(3*5)+(2*4)+(1*1)=112
112 % 10 = 2
So 144425-41-2 is a valid CAS Registry Number.

144425-41-2Downstream Products

144425-41-2Relevant academic research and scientific papers

New Building Blocks, 3,5-Dihydro-1H-thienopyrrole 2,2-Dioxides; Preparation and their Diels-Alder Reaction with Dimethyl Acetylenedicarboxylate

Ando, Kaori,Kankake, Mutsuo,Suzuki, Takayoshi,Takayama, Hiroaki

, p. 129 - 138 (2007/10/02)

New building blocks, 3,5-dihydro-1H-thienopyrrole 2,2-dioxides 3, have been prepared by the oxidation of their corresponding pyrroline derivates 4 with DDQ or Chemical MnO2.The Diels-Alder reaction of 3 with dimethyl acetylenedicarboxylate gave new types of compounds: 7-aza-2,3-dimethylenenorbornenes A, the 1:2 adducts B, 1a,3a,6,9-tetrahydrobenzindoles C, and dihydroindolosulfolene D depending on the reaction conditions and the N-substituents.The reaction of 3 with bis(tert-butylsulfonyl)acetylene was also described.

New Building Blocks, 3,5-Dihydro-1H-thienopyrrole 2,2-Dioxides; Preparation and their Diels-Alder Reaction with Dimethyl Acetylenedicarboxylate

Ando, Kaori,Kankake, Mutuo,Suzuki, Takayoshi,Takayama, Hiroaki

, p. 1100 - 1102 (2007/10/02)

New building blocks, 3,5-dihydro-1H-thienopyrrole 2,2-dioxides 1, have been prepared and react with dimethyl acetylenedicarboxylate to give new types of compound; 7-aza-2,3-dimethylenenorbornene A, the 1 : 2 adduct B, 1a,3a,6,9-tetrahydrobenzindole C, and dihydroindolosulfolene D depending on the reaction conditions and the N-substituent.

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