Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Benzoyl chloride, 2-propyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63620-04-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 63620-04-2 Structure
  • Basic information

    1. Product Name: Benzoyl chloride, 2-propyl- (9CI)
    2. Synonyms: Benzoyl chloride, 2-propyl- (9CI)
    3. CAS NO:63620-04-2
    4. Molecular Formula: C10H11ClO
    5. Molecular Weight: 182.64674
    6. EINECS: N/A
    7. Product Categories: ACIDHALIDE
    8. Mol File: 63620-04-2.mol
  • 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: Benzoyl chloride, 2-propyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoyl chloride, 2-propyl- (9CI)(63620-04-2)
    11. EPA Substance Registry System: Benzoyl chloride, 2-propyl- (9CI)(63620-04-2)
  • 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: 63620-04-2(Hazardous Substances Data)

63620-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63620-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,2 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63620-04:
(7*6)+(6*3)+(5*6)+(4*2)+(3*0)+(2*0)+(1*4)=102
102 % 10 = 2
So 63620-04-2 is a valid CAS Registry Number.

63620-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propylbenzoyl chloride

1.2 Other means of identification

Product number -
Other names 2-PROPYL-BENZOYL CHLORIDE

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:63620-04-2 SDS

63620-04-2Relevant articles and documents

N-Heterocyclic-Carbene-Catalyzed C–H Acylation via Radical Relay

Liu, Shiwen,Man, Yunquan,Xu, Bo,Zeng, Xiaojun

supporting information, p. 944 - 948 (2022/02/05)

A method of N-fluorocarboxamide-directed N-heterocyclic-carbene (NHC)-catalyzed benzylic C–H acylation with aldehydes via the hydrogen atom transfer strategy is disclosed. This transformation involves a sequence of single-electron transfer, 1,5-hydrogen a

Copper-catalyzed aerobic double functionalization of benzylic C(sp3)-H bonds for the synthesis of 3-hydroxyisoindolinones

Nozawa-Kumada, Kanako,Matsuzawa, Yuta,Ono, Kanako,Shigeno, Masanori,Kondo, Yoshinori

supporting information, p. 8604 - 8607 (2021/09/02)

A copper-catalyzed aerobic 3-hydroxyisoindolinone synthesis was developed via the benzylic double C(sp3)-H functionalization of 2-alkylbenzamides. In this reaction, molecular oxygen was used as both an oxidant for C(sp3)-H functionalization and an oxygen source. Our method can be extended to diverse benzylic C(sp3)-H bonds and shows excellent functional group tolerance. This journal is

Protoberberins from Reissert Compounds VI [1]. Diastereoselective Synthesis and Relative Configuration of 2-Benzoyl-1-cyano-1-(1-phenylalkyl)-1,2-dihydroisoquinolines

Reimann, Eberhard,Erdle, Wolfgang,Weigl, Claudia,Polborn, Kurt

, p. 313 - 326 (2007/10/03)

The alkylation of Reissert compounds 8 by sec-benzyl bromides 4, 7, and 10 diastereoselectively affords the title compounds 11 and 12. X-Ray structure analysis confirms an opposite configuration of the chiral centers in 11 and 12. The benzyl bromides 4, 7, and 10 are prepared by standard procedures.

The Reactions of Carbene Intermediates from the Reaction of Trialkyl Phosphites with Dialkyl Benzoylphosphonates: Intramolecular Cyclisations of 2-Substituted Dialkyl Benzoylphosphonates

Griffiths, D. Vaughan,Griffiths, Penelope A.,Karim, Khalku,Whitehead, Belinda J.

, p. 901 - 925 (2007/10/03)

The reaction of dialkyl aroylphosphonates 1 with trialkyl phosphites leads to the formation of carbene intermediates 3 via the anionic intermediates 2.The carbene intermediates 3 (R = 2-Me, 2-Prn, 2-Bun, 2-MeS, 2-EtO and 2-EtS) have

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 63620-04-2