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BIO-FARMA BF002831 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 824961-53-7 Structure
  • Basic information

    1. Product Name: BIO-FARMA BF002831
    2. Synonyms: CHEMBRDG-BB 7927733;BIO-FARMA BF002831;5-(4-CHLOROPHENYL)-1-METHYL-1H-PYRROLE-2-CARBALDEHYDE;5-(4-chlorophenyl)-1-methyl-1H-pyrrole-2-carbaldehyde(SALTDATA: FREE)
    3. CAS NO:824961-53-7
    4. Molecular Formula: C12H10ClNO
    5. Molecular Weight: 219.67
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 824961-53-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 360.8°C at 760 mmHg
    3. Flash Point: 172°C
    4. Appearance: /
    5. Density: 1.18g/cm3
    6. Vapor Pressure: 2.17E-05mmHg at 25°C
    7. Refractive Index: 1.583
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: BIO-FARMA BF002831(CAS DataBase Reference)
    11. NIST Chemistry Reference: BIO-FARMA BF002831(824961-53-7)
    12. EPA Substance Registry System: BIO-FARMA BF002831(824961-53-7)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-36-43
    3. Safety Statements: 26-36/37
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 824961-53-7(Hazardous Substances Data)

824961-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 824961-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,9,6 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 824961-53:
(8*8)+(7*2)+(6*4)+(5*9)+(4*6)+(3*1)+(2*5)+(1*3)=187
187 % 10 = 7
So 824961-53-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H10ClNO/c1-14-11(8-15)6-7-12(14)9-2-4-10(13)5-3-9/h2-8H,1H3

824961-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-chlorophenyl)-1-methylpyrrole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:824961-53-7 SDS

824961-53-7Upstream product

824961-53-7Downstream Products

824961-53-7Relevant articles and documents

Preparation method of pyrrole aldehyde compound

-

Paragraph 0059-0062; 0091-0094, (2020/08/02)

The invention discloses a preparation method of a pyrrole aldehyde compound, and relates to the technical field of compound preparation. According to the method, initial materials are mixed and react,wherein the initial materials comprise a substituted pyridine quaternary ammonium salt, an iodine source, an alkali and water, the structural formula of the substituted pyridine quaternary ammonium salt is defined in the specification, the substituent R is at the ortho-position and/or meta-position of a nitrogen atom, R is alkyl, aryl, heteroaryl or halogen, and the substituent R3 is alkyl or benzyl. The method is simple to operate, raw materials are easy to obtain, the chemical selectivity is good, few byproducts are produced, a substrate can be converted into various other useful molecules,the method has high practicability compared with the existing preparation of the pyrrole aldehyde compound, and the yield can reach 86% at most.

Synthesis of 2-Formylpyrroles from Pyridinium Iodide Salts

Xu, Ke,Li, Wenjing,Sun, Rui,Luo, Lihua,Chen, Xue,Zhang, Chunchun,Zheng, Xueli,Yuan, Maolin,Fu, Haiyan,Li, Ruixiang,Chen, Hua

, p. 6107 - 6111 (2020/08/12)

The first I2-mediated synthesis of 2-formylpyrroles from pyridinium salts is reported. This protocol enables the synthesis of diversely substituted 2-formylpyrroles in good yields under operationally simple conditions. The detailed mechanistic studies reveal that the reaction proceeds via a novel H2O-triggered ring opening of the pyridinium salt and a subsequent intramolecularly nucleophilic addition sequence.

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