15115-76-1

• 

• Basic information

  1. Product Name: 4-[(4-bromophenyl)sulfanyl]butanoic acid
  2. Synonyms:
  3. CAS NO:15115-76-1
  4. Molecular Formula: C₁₀H₁₁BrO₂S
  5. Molecular Weight: 275.1621
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15115-76-1.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 410.1°C at 760 mmHg
  3. Flash Point: 201.8°C
  4. Appearance: N/A
  5. Density: 1.54g/cm³
  6. Vapor Pressure: 1.84E-07mmHg at 25°C
  7. Refractive Index: 1.623
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 4-[(4-bromophenyl)sulfanyl]butanoic acid(CAS DataBase Reference)
  11. NIST Chemistry Reference: 4-[(4-bromophenyl)sulfanyl]butanoic acid(15115-76-1)
  12. EPA Substance Registry System: 4-[(4-bromophenyl)sulfanyl]butanoic acid(15115-76-1)

• 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: 15115-76-1(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• Butanoic acid,4-[(4-bromophenyl)thio]-

  Cas No: 15115-76-1

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• Butanoic acid,4-[(4-bromophenyl)thio]- cas 15115-76-1

  Cas No: 15115-76-1

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15115-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15115-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,1 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15115-76:
(7*1)+(6*5)+(5*1)+(4*1)+(3*5)+(2*7)+(1*6)=81
81 % 10 = 1
So 15115-76-1 is a valid CAS Registry Number.

15115-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-(4-bromophenyl)sulfanylbutanoic acid

1.2 Other means of identification

Product number	-
Other names	4-[(4-bromophenyl)sulfanyl]butanoic acid

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:15115-76-1 SDS

15115-76-1Upstream product

• 106-53-6 para-bromobenzenethiol 
• 15085-43-5 4-(4-bromophenylsulfanyl)butyric acid ethyl ester 

15115-76-1Downstream Products

• 229005-68-9 7-(4-methylphenyl)-N-(4-{[methyl(tetrahydro-2H-pyran-4-yl)amino]methyl}phenyl)-2,3-dihydro-1-benzothiepine-4-carboxamide 
• 279261-60-8 7-(4-methylphenyl)-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylic acid 
• 279261-59-5 methyl 7-(4-methylphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate 1,1-dioxide 
• 259739-46-3 7-(4-methylphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylic acid 
• 677707-98-1 methyl 7-(4-methylphenyl)-5-oxo-2,3,4,5-tetrahydro-1-benzothiepine-4-carboxylate 
• 279263-09-1 methyl 7-(4-methylphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate 
• 677707-97-0 7-(4-methylphenyl)-3,4-dihydro-1-benzothiepin-5(2H)-one 
• 15084-55-6 7-bromo-3,4-dihydro-1-benzothiepin-5(2H)-one 

15115-76-1Relevant articles and documents

Synthesis of 1-benzothiepine and 1-benzazepine derivatives as orally active CCR5 antagonists

Aramaki, Yoshio,Seto, Masaki,Okawa, Tomohiro,Oda, Tsuneo,Kanzaki, Naoyuki,Shiraishi, Mitsuru

, p. 254 - 258 (2007/10/03)

Quaternary ammonium benzocycloheptene compound 1 has previously been reported as a clinical candidate for an injectable CCR5 antagonist. In order to develop an orally active CCR5 antagonist, derivatives of tertiary amine benzocycloheptene 2, the chemical precursor to 1, were investigated. The benzocycloheptene ring was converted to benzothiepine and benzazepine rings and it was found that these changes could enhance the potency of tertiary amine derivatives. In particular, the 1-benzothiepine-1,1-dioxide 11b and the N-methyl-1-benzazepine 18 showed increased activity and good preliminary pharmacokinetic properties. The synthesis of 1-benzothiepine and 1-benzazepine derivatives and their activity are described.

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