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2-(benzylthio)-3-(4-methoxyphenyl)quinazolin-4(3H)-one is a complex organic compound belonging to the quinazolinone class, characterized by a fused benzene ring and a quinazoline core. This molecule features a benzylthio group at the 2-position, which is a benzyl group attached to a sulfur atom, and a 4-methoxyphenyl group at the 3-position, which is a phenyl ring with a methoxy substituent at the 4-position. The compound has a 4(3H)-one functional group, indicating a ketone at the 4-position with a hydrogen atom attached to the adjacent carbon, forming a 3H-quinazolin-4-one structure. This chemical is known for its potential applications in medicinal chemistry, particularly as a precursor or intermediate in the synthesis of various bioactive molecules.

1688-87-5

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1688-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1688-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1688-87:
(6*1)+(5*6)+(4*8)+(3*8)+(2*8)+(1*7)=115
115 % 10 = 5
So 1688-87-5 is a valid CAS Registry Number.

1688-87-5Downstream Products

1688-87-5Relevant academic research and scientific papers

Integrated one-flow synthesis of heterocyclic thioquinazolinones through serial microreactions with two organolithium intermediates

Kim, Heejin,Lee, Hyune-Jea,Kim, Dong-Pyo

, p. 1877 - 1880 (2015)

The synthesis of pharmaceutical compounds via short-lived intermediates in a microreactor is attractive, because of the fast flow and high throughput. Additionally, intermediates can be utilized sequentially to efficiently build up a library in a short time. Here we present an integrated microfluidic synthesis of biologically active thioquinazolinone libraries. Generation of o-lithiophenyl isothiocyanate and subsequent reaction with aryl isocyanate is optimized by controlling the residence time in the microreactor to 16 ms at room temperature. Various S-benzylic thioquinazolinone derivatives are synthesized within 10 s in high yields (75-98%) at room temperature. These three-step reactions involve two organolithium intermediates, an isothiocyanate-functionalized aryllithium intermediate, and a subsequent lithium thiolate intermediate. We also demonstrate the gram-scale synthesis of a multifunctionalized thioquinazolinone in the microfluidic device with a high yield (91%) and productivity (1.25 g in 5 min).

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