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4-chloro-1-(chloromethyl)-2-methylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16470-09-0 Structure
  • Basic information

    1. Product Name: 4-chloro-1-(chloromethyl)-2-methylbenzene
    2. Synonyms: 4-chloro-1-(chloromethyl)-2-methylbenzene
    3. CAS NO:16470-09-0
    4. Molecular Formula: C8H8Cl2
    5. Molecular Weight: 175.05512
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16470-09-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 87 °C(Press: 0.1 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.204±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-chloro-1-(chloromethyl)-2-methylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-chloro-1-(chloromethyl)-2-methylbenzene(16470-09-0)
    11. EPA Substance Registry System: 4-chloro-1-(chloromethyl)-2-methylbenzene(16470-09-0)
  • 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: 16470-09-0(Hazardous Substances Data)

16470-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16470-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,7 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16470-09:
(7*1)+(6*6)+(5*4)+(4*7)+(3*0)+(2*0)+(1*9)=100
100 % 10 = 0
So 16470-09-0 is a valid CAS Registry Number.

16470-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-1-(chloromethyl)-2-methylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,4-chloro-1-(chloromethyl)-2-methyl

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:16470-09-0 SDS

16470-09-0Relevant articles and documents

LONIDAMINE ANALOGUES FOR FERTILITY MANAGEMENT

-

Page/Page column 69, (2011/02/24)

Fertility management can include: administering to the subject one or more doses of a compound according to Formula I so as to reduce fertility in the subject. Fertility management can also include administering an effective amount of the compound to: impair Sertoli cell function in a male subject; inhibit spermatogenesis in the subject; reduce testis weight in the subject; reduce ovary weight in a female subject; reduce serum progesterone in the female subject; impair ovarian follicle function in the female subject; causing reversible fertility in the subject. In order to return fertility, the method can include ceasing administration of the compound to the subject so as to return fertility in the subject. The compound can be administered for irreversibly sterilizing the subject.

Esters of 2-phenylalkanenitriles and antifungal compositions containing them

-

, (2008/12/06)

Esters of 2-phenylalkanenitriles, such as 3-acetoxy-2-(2-chloro-5-(difluoromethoxy)phenyl)propanenitrile and 3-acetoxy-2-(4-chlorophenyl)propanenitrile, and compositions containing such esters, are useful as fungicides at very low concentrations.

Lonidamine analogues and their use in male contraception and cancer treatment

-

, (2008/06/13)

Novel compounds useful for inhibiting spermatogenesis and cancer treatment, and in particular as inhibitors of heat shock proteins and/or elongation factor 1 alpha.

SELECTIVITY AND MECHANISM IN THE SIDE-CHAIN HALOGENATION OF METHYLBENZENES PROMOTED PHOTOCHEMICALLY AND BY METAL COMPLEXES IN THE PRESENCE OF HALIDE IONS

Baciocchi, Enrico,Crescenzi, Manuela

, p. 6525 - 6536 (2007/10/02)

The intramolecular selectivity in a variety of side-chain halogenations of alkyl-aromatics has been determined in AcOH by measuring the isomeric distribution in the reactions of 4-t-butyl- and 4-chloro-1,2-dimethylbenzene (1 and 2, respectively) with: Br2/hν, CAN/Br-, CAN=cerium(IV) ammonium nitrate, cobalt(III) acetate/Br-, S2O8=/Br-, N-bromosuccinimide (in CCl4), Cl2/hν, CAN/Cl-, cobalt(III) acetate/Cl-.In the bromination reactions selectivity is independent of the reaction conditions, thus suggesting that in all brominating systems Br. is the actual reacting species.Very surprisingly, with 1 as the substrate, Cl2/hν is a more selective system than Br2/hν.With 2 the two systems display similar selectivity.It has been suggested that in AcOH the transition state for photochlorination has an electron transfer character which increases as the substrate becomes more electron rich.The idea of a "variable" transition state for the photochlorination in AcOH is supported by data of relative reactivity of substituted toluenes indicating that the effect on the rate increases as the substituent becomes more electron donor.AcOH must have an essential role in this respect since in CCl4 situation returns to be "normal" with chlorination less selective than bromination.Selectivity of CAN/Cl- is very similar to that of Cl2/hν, whereas significant differences are observed with cobalt(III) acetate/Cl-.Probably Cl. and a cobalt(III) chloride complex are the reacting species in CAN/Cl- and cobalt(III) acetate/Cl-, respectively.

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