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racemic 2-((1-phenylethyl)thio)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20803-99-0

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20803-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20803-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,0 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20803-99:
(7*2)+(6*0)+(5*8)+(4*0)+(3*3)+(2*9)+(1*9)=90
90 % 10 = 0
So 20803-99-0 is a valid CAS Registry Number.

20803-99-0Relevant academic research and scientific papers

MUSCARINIC ACETYLCHOLINE M1 RECEPTOR ANTAGONISTS

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Paragraph 0484; 0486, (2021/04/17)

Provided herein, inter alia, are compounds which are useful as antagonists of the muscarinic acetylcholine receptor M1 (mAChR M1); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions.

Highly Efficient and Chemoselective Tertiary and Secondary Benzylation of Thiols Catalyzed by Indium(III) Triflate

Kuciński, Krzysztof,Hreczycho, Grzegorz

, p. 5572 - 5581 (2017/10/13)

Several examples of nucleophilic substitution reactions of compounds that have good leaving groups have been previously reported, but the direct use of simple alcohols still remains a challenge because of the poor leaving ability of the hydroxy group. Herein, an efficient and highly chemoselective method for the S-benzylation of a wide range of aromatic and aliphatic thiols has been accomplished in the presence of catalytic amounts (0.1–0.2 mol-%) of indium(III) triflate. Our approach is atom efficient (water is the only byproduct) and suitable to obtain the corresponding unsymmetrical thioethers in excellent yields (up to 99 %). The low loading of catalyst that are needed to obtain extraordinarily high chemoselectivities and the generality of the reaction make this approach unique.

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