115104-25-1

• 

• Basic information

  1. Product Name: 2-(BROMOMETHYL)-7-CHLOROQUINOLINE
  2. Synonyms: 2-(BROMOMETHYL)-7-CHLOROQUINOLINE
  3. CAS NO:115104-25-1
  4. Molecular Formula: C₁₀H₇BrClN
  5. Molecular Weight: 256.52628
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 115104-25-1.mol
  9. Article Data: 9

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 334.7 °C at 760 mmHg
  3. Flash Point: 156.2 °C
  4. Appearance: /
  5. Density: 1.621 g/cm³
  6. Refractive Index: N/A
  7. Storage Temp.: 2-8°C
  8. Solubility: N/A
  9. PKA: 1.53±0.50(Predicted)
  10. CAS DataBase Reference: 2-(BROMOMETHYL)-7-CHLOROQUINOLINE(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-(BROMOMETHYL)-7-CHLOROQUINOLINE(115104-25-1)
  12. EPA Substance Registry System: 2-(BROMOMETHYL)-7-CHLOROQUINOLINE(115104-25-1)

• 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: 115104-25-1(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• 2-(BROMOMETHYL)-7-CHLOROQUINOLINE

  Cas No: 115104-25-1

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• Quinoline,2-(bromomethyl)-7-chloro-

  Cas No: 115104-25-1

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• 10 Gram

• 500 Kilogram/Month

• Zibo Hangyu Biotechnology Development Co., Ltd
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• 115104-25-1

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• Suzhou Health Chemicals Co., Ltd.
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• Quinoline,2-(bromomethyl)-7-chloro-

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• 2-(BROMOMETHYL)-7-CHLOROQUINOLINE

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• Chemlyte Solutions
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• 2-(BROMOMETHYL)-7-CHLOROQUINOLINE

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• 2-(Bromomethyl)-7-chloroquinoline

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• ENAO Chemical Co, Limited
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• 2-(BROMOMETHYL)-7-CHLOROQUINOLINE

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• Skyrun Industrial Co.,Ltd
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• Quinoline,2-(bromomethyl)-7-chloro-

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• 2-(BROMOMETHYL)-7-CHLOROQUINOLINE

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115104-25-1 Usage

General Description

"2-(Bromomethyl)-7-chloroquinoline" is a chemical compound that consists of a quinoline ring with bromomethyl and chloro substituents at the 2 and 7 positions, respectively. It is used in various chemical reactions and organic syntheses as a reagent or precursor. 2-(BROMOMETHYL)-7-CHLOROQUINOLINE may also have potential applications in pharmaceutical research due to its structural features and potential biological activities. Its unique structure and reactivity make it a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, its chloro and bromo groups make it an interesting target for substitution reactions and other chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 115104-25-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,0 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115104-25:
(8*1)+(7*1)+(6*5)+(5*1)+(4*0)+(3*4)+(2*2)+(1*5)=71
71 % 10 = 1
So 115104-25-1 is a valid CAS Registry Number.

115104-25-1SDS

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	2-(BROMOMETHYL)-7-CHLOROQUINOLINE

1.2 Other means of identification

Product number	-
Other names	QC-911

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:115104-25-1 SDS

115104-25-1Upstream product

• 4965-33-7 2-methyl-7-chloroquinoline 
• 34241-39-9 azobisisobutyronitrile 
• 94-36-0 dibenzoyl peroxide 
• 168083-35-0 2-(bromomethyl)-6-fluoroquinoline 

115104-25-1Downstream Products

• 150320-29-9 Methyl 3-methoxy-4-(5-nitro-1-(7-chloroquinolin-2-ylmethyl)indol-3-yl)methylbenzoate 
• 168083-07-6 3-(7-chloro-2-quinolinylmethoxy)aniline 
• 115104-36-4 3-<<(7-chloro-2-quinolinyl)methyl>thio>benzaldehyde 
• 133772-64-2 Methyl 5-chloro-2-(3-(3-((7-chloro-2-quinolinyl)methoxy)phenyl)-3-hydroxy propyl) benzoate 
• 115104-30-8 3-((7-chloroquinolin-2-ylmethyl)oxy)benzaldehyde 
• 115104-27-3 3-[{3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenyl}-(2-dimethylcarbamoyl-ethylsulfanyl)-methylsulfanyl]-propionic acid methyl ester 
• 115104-27-3 3-[{3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenyl}-(2-dimethylcarbamoyl-ethylsulfanyl)-methylsulfanyl]-propionic acid methyl ester 
• 115104-28-4 (-)-L-660,711 
• 115104-28-4 (+)-L-660,711 
• 138786-54-6 2-<<5-<3-<(7-chloroquinolin-2-yl)methoxy>phenyl>-2H-tetrazol-2-yl>methyl>benzoic acid methyl ester 
• 138786-52-4 2-{5-[3-(7-Chloro-quinolin-2-ylmethoxy)-phenyl]-tetrazol-2-ylmethyl}-benzoic acid 
• 138786-14-8 7-chloro-2-<<3-(2H-tetrazol-5-yl)phenoxy>methyl>quinoline 
• 121702-00-9 3-<<<3-<2-(7-chloro-2-quinolinyl)-(E)-ethenyl>phenyl><<3-(dimethylamino)-3-oxopropyl>thio>methyl>thio>propanoic acid 
• 1027926-74-4 3-[{3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenyl}-(3-morpholin-4-yl-3-oxo-propylsulfanyl)-methylsulfanyl]-propionic acid methyl ester 

115104-25-1Relevant articles and documents

Novel N-acylated heterocycles

-

, (2008/06/13)

Described are compositions comprising a muscarinic receptor antagonist and an N-acylated heterocycle derivative having affinity for serotonergic receptors, and enantiomers, diastereoisomers, N-oxides, polymorphs, solvates and pharmaceutically acceptable salts thereof. The combination of a muscarinic receptor antagonist and an N-acylated heterocycle, or an enantiomer, diastereoisomer, N-oxide, polymorph, solvate or pharmaceutically acceptable salt thereof, is useful in the treatment of patients with neuromuscular dysfunction of the lower urinary tract and diseases related to 5-HT1A receptors.

Synthesis and SAR of a novel, potent and structurally simple LTD4 antagonist of the quinoline class

Von Sprecher, Andreas,Gerspacher, Marc,Beck, Andreas,Kimmel, Sabine,Wiestner, Hansruedi,Anderson, Gary P.,Niederhauser, Ulrich,Subramanian, Natarajan,Bray, Michael A.

, p. 965 - 970 (2007/10/03)

The two geminal ethyl groups in the succinic acid moiety of CGP57698 (4- [3-(7-fluoro-2-quinolinylmethoxy)phenyl-amino]-2,2-diethyl-4-oxo-butanoic acid) are responsible for the high in vitro and in vivo potency of this peptidoleukotriene antagonist of the quinoline type. The synthesis and structure activity relationships of CGP57698 and its analogs are described.

2-ANILINO PHENYLACETIC ACID DERIVATIVES

-

, (2008/06/13)

-

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