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Benzene, 1-chloro-4-(1-methylheptyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105824-44-0 Structure
  • Basic information

    1. Product Name: Benzene, 1-chloro-4-(1-methylheptyl)-
    2. Synonyms:
    3. CAS NO:105824-44-0
    4. Molecular Formula: C14H21Cl
    5. Molecular Weight: 224.774
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105824-44-0.mol
  • 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: Benzene, 1-chloro-4-(1-methylheptyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1-chloro-4-(1-methylheptyl)-(105824-44-0)
    11. EPA Substance Registry System: Benzene, 1-chloro-4-(1-methylheptyl)-(105824-44-0)
  • 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: 105824-44-0(Hazardous Substances Data)

105824-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105824-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,2 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105824-44:
(8*1)+(7*0)+(6*5)+(5*8)+(4*2)+(3*4)+(2*4)+(1*4)=110
110 % 10 = 0
So 105824-44-0 is a valid CAS Registry Number.

105824-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chloro-phenyl)-octane

1.2 Other means of identification

Product number -
Other names Methyl-hexyl-<4-chlor-phenyl>-methan

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:105824-44-0 SDS

105824-44-0Downstream Products

105824-44-0Relevant articles and documents

Iron(II)-Catalyzed Site-Selective Functionalization of Unactivated C(sp3)?H Bonds Guided by Alkoxyl Radicals

Guan, Honghao,Sun, Shutao,Mao, Ying,Chen, Lei,Lu, Ran,Huang, Jiancheng,Liu, Lei

supporting information, p. 11413 - 11417 (2018/08/28)

An alkoxyl radical guided strategy for site-selective functionalization of unactivated methylene and methine C?H bonds enabled by an FeII-catalyzed redox process is described. The mild, expeditious, and modular protocol allows efficient remote aliphatic fluorination, chlorination, amination, and alkynylation of structurally and electronically varied primary, secondary, and tertiary hydroperoxides with excellent functional-group tolerance. The application for one-pot 1,4-hydroxyl functionalization of non-oxygenated alkane substrates initiated by aerobic C?H oxygenation is also demonstrated.

A NOVEL METHOD FOR THE GEMINAL DIALKYLATION OF THE CARBONYL GROUP OF AROMATIC ALDEHYDES AND KETONES

Clarembeau, M.,Krief, A.

, p. 1719 - 1722 (2007/10/02)

The title transformation is efficiently achieved by using the selenium methodology which involves the sequential reductive alkylation of arylselenoacetals and of benzylselenides.

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