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(1S,4S,5S)-4-Ethyl-6,7-dioxa-bicyclo[3.2.2]nona-2,8-diene is a complex organic compound with a unique molecular structure. It is characterized by a bicyclic arrangement of carbon and oxygen atoms, with a double bond between the 6th and 7th carbon atoms. The compound has three chiral centers, which are the 1st, 4th, and 5th carbon atoms, all of which have the S configuration. The presence of an ethyl group at the 4th carbon atom further distinguishes (1S,4S,5S)-4-Ethyl-6,7-dioxa-bicyclo[3.2.2]nona-2,8-diene. It is a colorless liquid with a molecular formula of C9H12O2 and a molecular weight of 152.19 g/mol. (1S,4S,5S)-4-Ethyl-6,7-dioxa-bicyclo[3.2.2]nona-2,8-diene is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and other chemical products.

76778-60-4

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76778-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76778-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76778-60:
(7*7)+(6*6)+(5*7)+(4*7)+(3*8)+(2*6)+(1*0)=184
184 % 10 = 4
So 76778-60-4 is a valid CAS Registry Number.

76778-60-4Downstream Products

76778-60-4Relevant academic research and scientific papers

PHOTOOXYGENATION OF 7-SUBSTITUTED CYCLOHEPTATRIENES

Asao, Toyonobu,Yagihara, Morio,Kitahara, Yoshio

, p. 985 - 991 (2007/10/02)

Photooxygenation of 7-substituted cycloheptatrienes, including the Me, Et, iPr, Ph, CN, COOMe, COOEt, and CONH2 groups was studied, and several products among the tropilidene-type (1 and 2) and norcaradiene-type (3 and 4) endoperoxides, o-substituted benzaldehydes (5), diepoxides (6 and 7), and ketoalcohols (8) were obtained.Mechanism of the formations of the products was discussed.Thermal isomerization of the endoperoxides (1, 3 and 4) to the corresponding diepoxides (10, 6 and 7), and the reaction of the endoperoxides (1 and 3) with triethylamine were examined.

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