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22699-30-5

4-[(2,2-dimethylhydrazinyl)methylidene]cyclohexa-2,5-dien-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22699-30-5 Structure

  • Basic information

    1. Product Name: 4-[(2,2-dimethylhydrazinyl)methylidene]cyclohexa-2,5-dien-1-one
    2. Synonyms: 4-[(2,2-dimethylhydrazinyl)methylidene]cyclohexa-2,5-dien-1-one;p-Hydroxybenzaldehyde dimethyl hydrazone
    3. CAS NO:22699-30-5
    4. Molecular Formula: C9H12N2O
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22699-30-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 253.2°C at 760 mmHg
    3. Flash Point: 106.9°C
    4. Appearance: /
    5. Density: 1.178g/cm3
    6. Vapor Pressure: 0.0186mmHg at 25°C
    7. Refractive Index: 1.634
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-[(2,2-dimethylhydrazinyl)methylidene]cyclohexa-2,5-dien-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-[(2,2-dimethylhydrazinyl)methylidene]cyclohexa-2,5-dien-1-one(22699-30-5)
    12. EPA Substance Registry System: 4-[(2,2-dimethylhydrazinyl)methylidene]cyclohexa-2,5-dien-1-one(22699-30-5)

  • 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: 22699-30-5(Hazardous Substances Data)

22699-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22699-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,9 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22699-30:
(7*2)+(6*2)+(5*6)+(4*9)+(3*9)+(2*3)+(1*0)=125
125 % 10 = 5
So 22699-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O/c1-11(2)10-7-8-3-5-9(12)6-4-8/h3-7,10H,1-2H3

22699-30-5SDS

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 4-[(2,2-dimethylhydrazinyl)methylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names WLN: QR D1UNN1&4-Hydroxybenzaldehyde dimethylhydrazone

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:22699-30-5 SDS

22699-30-5Downstream Products

22699-30-5Relevant articles and documents

Perfluoroalkylation of Aryl-N,N-dimethyl Hydrazones Using Hypervalent Iodine(III) Reagents or Perfluoroalkyl Iodides

Janhsen, Benjamin,Studer, Armido

, p. 11703 - 11710 (2017/11/24)

Radical trifluoromethylation of aryl N,N-dimethyl hydrazones using TBAI as an initiator and Togni's reagent as a trifluoromethyl radical source is described. Cascades proceed via electron-catalysis; this approach is generally more applicable to hydrazone perfluoroalkylation using perfluoroalkyl iodides as the radical precursors in combination with a base under visible-light initiation.

REACTION PRODUCT OF HYDRAZINE DERIVATIVES AND CARBON DIOXIDE

-

Paragraph 0121-0122, (2015/04/15)

The present invention relates to the synthesis of a novel compound, in which liquid hydrazine and the derivatives thereof react with excess carbon dioxide to enable the carbon dioxide to chemically bond to the hydrazine and the derivatives thereof. To thi

Copper-catalyzed trifluoromethylation of N,N-dialkylhydrazones

Pair, Etienne,Monteiro, Nuno,Bouyssi, Didier,Baudoin, Olivier

supporting information, p. 5346 - 5349 (2013/06/05)

Mild and practical: Trifluoromethylation of (hetero)aromatic aldehyde N,N-dialkylhydrazones was achieved at room temperature by using Togni's trifluoromethylation reagent under CuCl catalysis (see scheme). This simple reaction is believed to occur by a CF3-radical-transfer mechanism and yields useful trifluoromethylated building blocks. Copyright

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