152074-07-2

• 

• Basic information

  1. Product Name: 2-BROMO-1-(2-ETHOXY-PHENYL)-ETHANONE
  2. Synonyms: 2-BROMO-1-(2-ETHOXY-PHENYL)-ETHANONE
  3. CAS NO:152074-07-2
  4. Molecular Formula: C₁₀H₁₁BrO₂
  5. Molecular Weight: 243.1
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 152074-07-2.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 2-BROMO-1-(2-ETHOXY-PHENYL)-ETHANONE(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2-BROMO-1-(2-ETHOXY-PHENYL)-ETHANONE(152074-07-2)
  11. EPA Substance Registry System: 2-BROMO-1-(2-ETHOXY-PHENYL)-ETHANONE(152074-07-2)

• 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: 152074-07-2(Hazardous Substances Data)

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• SDS
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• Article

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• 2-BROMO-1-(2-ETHOXY-PHENYL)-ETHANONE

  Cas No: 152074-07-2

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• Hangzhou Fandachem Co.,Ltd
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• Ethanone, 2-bromo-1-(2-ethoxyphenyl)-

  Cas No: 152074-07-2

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• SAGECHEM LIMITED
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152074-07-2 Usage

Uses

2-Bromo-1-(2-ethoxyphenyl)ethanone is used as a reagent in the preparation of aroylfurans and aroylthiophenes which are used in the treatment of neoplastic and autoimmune diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 152074-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,0,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 152074-07:
(8*1)+(7*5)+(6*2)+(5*0)+(4*7)+(3*4)+(2*0)+(1*7)=102
102 % 10 = 2
So 152074-07-2 is a valid CAS Registry Number.

152074-07-2SDS

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-Bromo-1-(2-ethoxyphenyl)ethanone

1.2 Other means of identification

Product number	-
Other names	2-bromo-2'-ethoxyacetophenone

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:152074-07-2 SDS

152074-07-2Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 2142-67-8 1-(2-ethoxyphenyl)ethanone 

152074-07-2Downstream Products

• 129486-35-7 4-(2-ethoxyphenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 

152074-07-2Relevant articles and documents

Discovery of novel potent GPR40 agonists containing imidazo[1,2-a]pyridine core as antidiabetic agents

Ye, Zhiwen,Liu, Chunxia,Zou, Feng,Cai, Yan,Chen, Bin,Zou, Yuxing,Mo, Jiaxian,Han, Ting,Huang, Wenlong,Qiu, Qianqian,Qian, Hai

, (2020/06/19)

Free fatty acid receptor 1 (FFA1 or GPR40) has been studied for many years as a target for the treatment of type 2 diabetes mellitus. In order to increase potency and reduce hepatotoxicity, a series of novel compounds containing imidazo[1,2-a]pyridine sca

Process for producing optically active carbinols

-

, (2008/06/13)

The present invention relates to a process for producing optically active halomethyl phenyl carbinols of the formula (1), comprising reducing halomethyl phenyl ketones of the formula (2) using an asymmetric reducing agent obtained from boranes and optically active α-phenyl-substituted-β-amino alcohols of the formula (3) or optically active α-non-substituted-β-amino alcohols of the formula (4). The present invention further relates to a process for producing optically active carbinols, comprising reacting a prochiral keytone with an asymmetric reducing agent obtained from optically active β-amino alcohols of the formula (5), a metal boron hydride and Lewis acid or lower dialkyl sulfuric acid. All of the formulas (1) to (5) are the same as shown in the specification.

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