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1-methyl-4-(2-methyldibenzo[b,e]thiepin-11(6H)-ylidene)tetrahydro-2H-thiopyranium iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1-methyl-4-(2-methyldibenzo[b,e]thiepin-11(6H)-ylidene)tetrahydro-2H-thiopyranium iodide

    Cas No: 116197-00-3

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  • 116197-00-3 Structure
  • Basic information

    1. Product Name: 1-methyl-4-(2-methyldibenzo[b,e]thiepin-11(6H)-ylidene)tetrahydro-2H-thiopyranium iodide
    2. Synonyms:
    3. CAS NO:116197-00-3
    4. Molecular Formula: C21H23IS2
    5. Molecular Weight: 466.4418
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116197-00-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-methyl-4-(2-methyldibenzo[b,e]thiepin-11(6H)-ylidene)tetrahydro-2H-thiopyranium iodide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methyl-4-(2-methyldibenzo[b,e]thiepin-11(6H)-ylidene)tetrahydro-2H-thiopyranium iodide(116197-00-3)
    11. EPA Substance Registry System: 1-methyl-4-(2-methyldibenzo[b,e]thiepin-11(6H)-ylidene)tetrahydro-2H-thiopyranium iodide(116197-00-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 116197-00-3(Hazardous Substances Data)

116197-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116197-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,9 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116197-00:
(8*1)+(7*1)+(6*6)+(5*1)+(4*9)+(3*7)+(2*0)+(1*0)=113
113 % 10 = 3
So 116197-00-3 is a valid CAS Registry Number.

116197-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-11-(1-methylthian-1-ium-4-ylidene)-6H-benzo[c][1]benzothiepine,iodide

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:116197-00-3 SDS

116197-00-3Downstream Products

116197-00-3Relevant articles and documents

POTENTIAL ANTIHISTAMINE AGENTS: 4-(6,11-DIHYDRODIBENZOTHIEPIN-11-YLIDENE)-1-METHYLTETRAHYDROTHIOPYRANIUM IODIDE AND SIMILAR SULFONIUM SALTS DERIVED FROM RELATED TRICYCLIC SYSTEMS

Polivka, Zdenek,Holubek, Jiri,Budesinsky, Milos,Matousova, Oluse,Svatek, Emil,et al.

, p. 2758 - 2774 (2007/10/02)

Thioxanthone, 10,11-dihydrodibenzocyclohepten-5-one, dibenzothiepin-11(6H)-one, its 2-methyl derivative, and thieno-2-benzothiepin-4(9H)-one were reacted with 4-tetrahydrothiopyranylmagnesium bromide and the obtained tertiary alcohols IVabc, VIc, and XIX were dehydrated to the olefinic sulfides IXabc, Xc, and XXI.Addition of methyl iodide afforded the title compounds XIabc, XIIc, and XXII.The Grignard reactions were accompanied by the 1,6-addition giving the ketones XVI-XVIII as by-products.The reductive properties of tetrahydrothiopyranylmagnesium bromide were most striking in the case of reaction with 2-chlorothioxanthone; the isolation of thioxanthene and thioxanthone showed that nuclear dehalogenation took also place.Reactions of 11-chloro-6,11-dihydrodibenzothiepin and benzhydryl chloride with tetrahydrothiopyran-4-ol gave the sulfides XXV and XXVIII; whereas the latter reacted with methyl iodide under the formation of sulfonium salt XXIX, the former was cleaved and gave 4-hydroxyl-1-methyltetrahydrothiopyranium iodide (XXVI).The sulfonium salts are free of the central effects but their antihistamine activity is rather low.

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