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2-(4-methoxyphenyl)-4-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

420809-56-9

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420809-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 420809-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,0,8,0 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 420809-56:
(8*4)+(7*2)+(6*0)+(5*8)+(4*0)+(3*9)+(2*5)+(1*6)=129
129 % 10 = 9
So 420809-56-9 is a valid CAS Registry Number.

420809-56-9Relevant academic research and scientific papers

Green protocol for synthesis of 1,5-benzodiazepines and 1,5-benzothiazepines in the presence of nanocrystalline aluminum oxide

Hekmatshoar, Rahim,Sadjadi, Sodeh,Shiri, Soudeh,Heravi, Majid M.,Beheshtiha, Yahya S.

experimental part, p. 2549 - 2559 (2009/12/04)

An efficient protocol associated with readily available starting materials, mild conditions, excellent yields, and a broad range of the products in synthetic chemistry was established for synthesis of 1,5-benzodiazepine and 1,5-benzothiazepine derivatives

Synthesis of 1,5-benzothiazepines with microwave irradiation under solvent and catalyst-free conditions

Rahman,Roy,Majee,Hajra

experimental part, p. 178 - 179 (2010/02/28)

Microwave irradiation of a,β-unsaturated ketones (chalcones) and o-aminothiophenol in the absence of solvent and catalyst provides a highly efficient methodology for the synthesis of 1,5-benzothiazepines in moderate to good yields.

'On water' synthesis of 2,4-diaryl-2,3-dihydro-1,5-benzothiazepines catalysed by sodium dodecyl sulfate (SDS)

Sharma, Gaurav,Kumar, Raj,Chakraborti, Asit K.

, p. 4269 - 4271 (2008/09/21)

An efficient synthesis of 1,3-diaryl-2,3-dihydro-1,5-benzothiazepines has been developed by the reaction of various 1,3-diaryl-2-propenones with 2-aminothiophenol in water under neutral conditions catalysed by SDS. Excellent chemoselectivity was observed for substrates possessing halogen atoms or nitro/alkoxy/thioalkyl groups which did not undergo competitive aromatic nucleophilic substitution of the halogen atoms or the nitro group, reduction of the nitro or the α,β-unsaturated carbonyl group, or dealkylation of the alkoxy/thioalkoxy groups.

Magnesium perchlorate as a new and highly efficient catalyst for the synthesis of 2,3-dihydro-1,5-benzothiazepines

Khatik, Gopal L.,Kumar, Raj,Chakraborti, Asit K.

, p. 541 - 546 (2007/12/29)

Commercially available magnesium perchlorate has been found to be a highly efficient catalyst for the reaction of 1,3-diarylprop-2-enones with 2-aminothiophenol leading to the synthesis of 2,3-dihydro-1,5-benzothiazepines in high yields and in short times. Georg Thieme Verlag Stuttgart.

A novel approach to tetrahydrobenzothiazepines from chalcones using o-aminothiophenol

Khanna, Mahavir S.,Kumar, Dalip,Garg, Chandra P.,Kapoor, Ram P.

, p. 333 - 335 (2007/10/02)

Synthesis of 2,3,4,5-tetrahydro-2,4-disubstituted phenyl-5H-benzothiazepines (2a-e) by the in situ reduction of 2,3-dihydro-2,4-disubstituted phenyl-5H-benzothiazepines (3a-e) using o-aminothiophenol in catalytic amount in acidic ethanol is desc

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