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191087-87-3

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191087-87-3 Usage

Type of medication

Antifungal

Uses

Treats a variety of fungal infections in the body, including athlete's foot, ringworm, and yeast infections

Mechanism of action

Prevents the growth and reproduction of fungal cells, leading to their destruction

Class

Azole antifungal

Additional potential uses

Investigated for its potential in treating certain types of cancer and Cushing's syndrome

Side effects

Known side effects and may interact with certain medications

Precautions

Should only be used under the guidance of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 191087-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,0,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 191087-87:
(8*1)+(7*9)+(6*1)+(5*0)+(4*8)+(3*7)+(2*8)+(1*7)=153
153 % 10 = 3
So 191087-87-3 is a valid CAS Registry Number.

191087-87-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-6-methyl-3,6-dihydropyridine-2(1H)-thione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:191087-87-3 SDS

191087-87-3Relevant articles and documents

Diastereoselective Michael Addition of Nitrogen and Sulfur-Nucleophiles to α,β-Unsaturated δ-Thiolactams

Sosnicki, Jacek G.,Jagodziriski, Tadeusz S.,Liebscher, Juergen

, p. 643 - 648 (2007/10/03)

5,6-Dihydropyridine-2-thiones 2 are synthesized from 5,6-dihydropyridin-2-ones 1 and Lawesson reagent. Stereoselective Michael-like addition of amines, methylhydrazine or functionalized thiols affords trans piperidine-2-thiones 5 with the corresponding heterosubstituent in position 4 as major products. The configuration of the adducts 5 was determined by nmr-techniques.

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