113425-30-2

• 

• Basic information

  1. Product Name: 1-Butanone, 4-chloro-1-(4-hydroxy-3-methylphenyl)-
  2. Synonyms:
  3. CAS NO:113425-30-2
  4. Molecular Formula: C11H13ClO2
  5. Molecular Weight: 212.676
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 113425-30-2.mol
  9. Article Data: 5

• 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-Butanone, 4-chloro-1-(4-hydroxy-3-methylphenyl)-(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1-Butanone, 4-chloro-1-(4-hydroxy-3-methylphenyl)-(113425-30-2)
  11. EPA Substance Registry System: 1-Butanone, 4-chloro-1-(4-hydroxy-3-methylphenyl)-(113425-30-2)

• 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: 113425-30-2(Hazardous Substances Data)

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• SDS
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• Downstream Products
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• 1-Butanone, 4-chloro-1-(4-hydroxy-3-methylphenyl)-

  Cas No: 113425-30-2

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113425-30-2 Usage

Type

Synthetic chemical compound

Usage

Commonly used in research and laboratory settings as a building block in the synthesis of various pharmaceuticals and organic compounds

Safety

Should be handled with caution and proper safety protocols must be followed to avoid hazards

Structure

Contains a butanone functional group with a 4-chloro substituent, a 4-hydroxy substituent on a methylphenyl ring, and a 3-methyl substituent on the ring.

Check Digit Verification of cas no

The CAS Registry Mumber 113425-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,2 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113425-30:
(8*1)+(7*1)+(6*3)+(5*4)+(4*2)+(3*5)+(2*3)+(1*0)=82
82 % 10 = 2
So 113425-30-2 is a valid CAS Registry Number.

113425-30-2SDS

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	4-chloro-1-(4-hydroxy-3-methylphenyl)butan-1-one

1.2 Other means of identification

Product number	-
Other names	1-Butanone,4-chloro-1-(4-hydroxy-3-methylphenyl)

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:113425-30-2 SDS

113425-30-2Upstream product

• 95-48-7 ortho-cresol 
• 4635-59-0 4-Chlorobutanoyl chloride 

113425-30-2Downstream Products

• 1083427-54-6 C₁₂H₁₅IO₂ 
• 1083427-51-3 C₁₂H₁₅ClO₂ 
• 1083427-48-8 C₁₁H₁₅ClO 
• 119837-40-0 2,2-Dichloro-1-[3-(4-hydroxy-3-methyl-phenyl)-5,6-dihydro-4H-pyridazin-1-yl]-ethanone 
• 119837-36-4 2-Methyl-4-(1,4,5,6-tetrahydro-pyridazin-3-yl)-phenol 

113425-30-2Relevant articles and documents

Study of electronic effect in bifunctional catalysts for the copolymerization of CO2 and PO/CHO

Hu, Yang,Du, Longchao,Li, Cun,Shen, Jiale,Zhu, Weiju,Shao, Chenxi

, p. 1818 - 1826 (2020)

Carbon dioxide (CO2) is an easily available renewable carbon source that can be used as a comonomer in the catalytic ring-opening polymerization of epoxides to form aliphatic polycarbonates. Herein, a series of new Salen-Co(III) bifunctional catalysts were synthesized for the first time, and they were studied to catalyze the copolymerization of CO2 and propylene oxide (PO)/cyclohexene oxide (CHO). At the same time, the effects of reaction conditions (electronic effect, temperature, time) on catalytic activity and selectivity were investigated. The results show that the Salen-Co(III) complexes with electron-withdrawing groups have higher selectivity and activity for propylene carbonate (PPC)/cyclohexylene carbonate (PCHC). At the same time, the Salen-Co(III) complexes can better catalyze the copolymerization of CHO and CO2 than that of PO and CO2. The catalytic efficiency of the four complexes increased with increasing temperature, and the best reaction condition is 80°C, 30 min and 2 MPa of CO2.

PROCESS FOR PRODUCING POLYCARBONATES AND A COORDINATION COMPLEX USED THEREFOR

-

Paragraph 0161, (2014/09/16)

The complex of the present invention containing an onium salt and a central Lewis acidic metal has a high catalytic activity at a high temperature for the copolymerization of an epoxide and carbon dioxide to produce a high molecular weight polycarbonate.

A GENERAL ROUTE TO 3-(HYDROXYARYL)TETRAHYDRO PYRIDAZINES AND 1,2-DIAZEPINES AND DERIVATIVES

Kalyanam, N.,Dave, K.G.,Likhate, M.A.

, p. 2183 - 2192 (2007/10/02)

A three step synthesis of 1-acyl-3-(hydroxyaryl)tetrahydro pyridazines and 1,2-diazepines starting from phenols is described.The hydrolytic lability of some intermediate chloroalkyl aryl ketones and a simple recovery of these ketones from nitrobenzene solution are indicated.

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