128439-98-5

Basic information

• Product Name: IX 207-887
• Synonyms: Aceticacid, (10-methoxy-4H-benzo[4,5]cyclohepta[1,2-b]thien-4-ylidene)- (9CI); 4H-Benzo[4,5]cyclohepta[1,2-b]thiophene,acetic acid deriv.; IX 207-887
• CAS NO: 128439-98-5
• Molecular Formula: C16H12O3S
• Molecular Weight: 284.32968
• Mol File: 128439-98-5.mol

Chemical Properties

• Boiling Point: 475°C at 760 mmHg
• Flash Point: 241.1°C
• Appearance: /
• Density: 1.37g/cm³
• Vapor Pressure: 7.91E-10mmHg at 25°C
• Refractive Index: 1.682
• CAS DataBase Reference: IX 207-887(CAS DataBase Reference)
• NIST Chemistry Reference: IX 207-887(128439-98-5)
• EPA Substance Registry System: IX 207-887(128439-98-5)

Safety Data

• Hazardous Substances Data: 128439-98-5(Hazardous Substances Data)

Usage

Uses

Used in Adhesives Industry:
IX 207-887 is used as a binding agent for creating strong and long-lasting bonds between different materials. Its excellent adhesive properties make it a popular choice in the adhesives industry.
Used in Coatings Industry:
IX 207-887 is used in the manufacturing of coatings to provide high strength, durability, and resistance to moisture, chemicals, and temperature fluctuations. This ensures the longevity and performance of the coatings in various applications.
Used in Sealants Industry:
IX 207-887 is utilized as a key component in sealants to form robust seals that resist environmental factors such as moisture, chemicals, and temperature changes. Its bonding capabilities contribute to the effectiveness and reliability of sealants in various industries.

InChI:InChI=1/C16H12O3S/c1-19-14-8-10-4-2-3-5-11(10)13(9-15(17)18)12-6-7-20-16(12)14/h2-9H,1H3,(H,17,18)/b13-9+

Upstream product

• 98320-26-4 [10-Methoxy-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-ylidene]-acetic acid methyl ester 
• 6322-85-6 6-Methoxy-7H-benzocyclohepten-7-on 
• 155788-39-9 8-Methoxy-7-oxo-7H-benzocyclohepten-5-essigsaeure-methylester 
• 155788-44-6 (E)-<7-<(Formylmethyl)thio>-8-methoxy-5H-benzocyclohepten-5-yliden>essigsaeure-methylester 
• 155788-43-5 (E)-<7-<(2,2-Diethoxyethyl)thio>-8-methoxy-5H-benzocyclohepten-5-yliden>essigsaeure-methylester 
• 155788-53-7 (E)-<7-<(2,2-Diisopropoxyethyl)thio>-8-methoxy-5H-benzocyclohepten-5-yliden>essigsaeure-methylester 
• 155788-42-4 (E)-<7-<(Diethoxyphosphoryl)oxy>-8-methoxy-5H-benzocyclohepten-5-yliden>essigsaeure-methylester 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 59743-84-9 10-methoxy-4H-benzo<4,5>cyclohepta<1,2-b>thiophen-4-one 
• 98320-27-5 methyl (10-methoxy-4H-benzo<4,5>cyclohepta<1,2-b>thiophen-4-ylidene)acetate 

Relevant articles and documents

Stereoselective syntheses of (Z)-(10-methoxy-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-ylidene)aceti c acid

Two stereoselective syntheses for the antiinflammatory compound 1 ((Z)-isomer) are described. In the first approach (Strategy A, Scheme 1) the stereoselective synthesis of 1 was realized via the bicyclic compound 11 under thermodynamic conditions, followe

4H-benzo(4,5)cyclohepta(1,2-B)thiophene derivatives

α-[5H-dibenzo[a,d]cyclohepten-5-ylidene]-carboxylic acids e.g. of formula I STR1 wherein R1 is H, C1-4 alkyl or phenyl-(C1-4 alkyl), R2 is H or C1-4 alkyl and ring A is unsubstituted or halo- or hydroxy-substituted, as well as the physiologically-hydrolysable and -acceptable esters thereof have valuable pharmaceutical, in particular anti-inflammatory, antipyretic and analgesic properties.