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4-CHLORO-4'-(DIMETHYLAMINO)BENZHYDROL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 844683-40-5 Structure
  • Basic information

    1. Product Name: 4-CHLORO-4'-(DIMETHYLAMINO)BENZHYDROL
    2. Synonyms: 4-CHLORO-4'-(DIMETHYLAMINO)BENZHYDROL
    3. CAS NO:844683-40-5
    4. Molecular Formula: C15H16ClNO
    5. Molecular Weight: 261.75
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 844683-40-5.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: 4-CHLORO-4'-(DIMETHYLAMINO)BENZHYDROL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-CHLORO-4'-(DIMETHYLAMINO)BENZHYDROL(844683-40-5)
    11. EPA Substance Registry System: 4-CHLORO-4'-(DIMETHYLAMINO)BENZHYDROL(844683-40-5)
  • 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: 844683-40-5(Hazardous Substances Data)

844683-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 844683-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,6,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 844683-40:
(8*8)+(7*4)+(6*4)+(5*6)+(4*8)+(3*3)+(2*4)+(1*0)=195
195 % 10 = 5
So 844683-40-5 is a valid CAS Registry Number.

844683-40-5Downstream Products

844683-40-5Relevant articles and documents

Bu4N+ alkoxide-initiated/autocatalytic addition reactions with organotrimethylsilanes

Das, Manas,O'Shea, Donal F.

, p. 5595 - 5607 (2014/07/08)

The use of Me3SiO-/Bu4N+ as a general activator of organotrimethylsilanes for addition reactions has been established. The broad scope of the method offers trimethylsilanes (including acetate, allyl, propargyl, benzyl, dithiane, heteroaryl, and aryl derivatives) as bench-stable organometallics that can be readily utilized as carbanion equivalents for synthesis. Reactions are achieved at rt without the requirement of specialized precautions that are commonplace for other organometallics.

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