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2-[(Diphenylmethyl)thio]acetamide

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Product Code: CS-O-31752 Intermediate
2-[(Diphenylmethyl)thio]acetamide
API Family
Modafinil
Product Code
CS-O-31752

2-[(Diphenylmethyl)thio]acetamide

Modafinil Intermediate
Stock Status: In Stock
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CAT No.
CS-O-31752
CAS No.
68524-30-1
Molecular Formula
C₁₅H₁₅NOS
Molecular Weight
257.35
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
68524-30-1
Product Code
CS-O-31752
M.F.
C₁₅H₁₅NOS
M.W.
257.35
Smiles
O=C(N)CSC(C1=CC=CC=C1)C2=CC=CC=C2
Category
Intermediate
API Family
Modafinil
Storage Condition
Store at refrigerator (2-8°C) for long term storage
IUPAC Name
2-(benzhydrylthio)acetamide
References
CAS
PubChem
Wikipedia
Synonyms
2-(benzhydrylthio)acetamide
Application Notes
" Deoxy Modafinil is an analogue and precursor to Modafinil (M482500), an a-1-adrenergic agonist. Modafinil is a CNS stimulant; psychostimulant that displays neuroprotective and antiparkinsonian activity in a primate model of Parkinson’s disease." " Saletu, B,, et al,: Int, J, Clin, Pharmacol, Res,, 9, 183 (1989), Chemelli, R,M,, et al,: Cell, 98, 437 (1999), Purnell, M,, et al,: J, Sleep Res,, 11, 219 (2002); Okunola-Bakare, O, et al,: J, Med, Chem,, 57, 1000 (2014); Olivo, H, et al,: Tetrah"
Purity by HPLC
Not less than 90%
Hazard Compound
Refer MSDS for accurate information.
Overview
" Deoxy Modafinil is an analogue and precursor to Modafinil (M482500), an a-1-adrenergic agonist. Modafinil is a CNS stimulant; psychostimulant that displays neuroprotective and antiparkinsonian activity in a primate model of Parkinson’s disease." " Saletu, B,, et al,: Int, J, Clin, Pharmacol, Res,, 9, 183 (1989), Chemelli, R,M,, et al,: Cell, 98, 437 (1999), Purnell, M,, et al,: J, Sleep Res,, 11, 219 (2002); Okunola-Bakare, O, et al,: J, Med, Chem,, 57, 1000 (2014); Olivo, H, et al,: Tetrah"

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