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2-bromo-3-hydroxy-5,5-dimethylcyclohex-2-en-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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  • 37722-34-2 Structure
  • Basic information

    1. Product Name: 2-bromo-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one
    2. Synonyms:
    3. CAS NO:37722-34-2
    4. Molecular Formula: C8H11BrO2
    5. Molecular Weight: 219.0757
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37722-34-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 253.8°C at 760 mmHg
    3. Flash Point: 107.3°C
    4. Appearance: N/A
    5. Density: 1.542g/cm3
    6. Vapor Pressure: 0.00276mmHg at 25°C
    7. Refractive Index: 1.562
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-bromo-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-bromo-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one(37722-34-2)
    12. EPA Substance Registry System: 2-bromo-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one(37722-34-2)
  • 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: 37722-34-2(Hazardous Substances Data)

37722-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37722-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,2 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37722-34:
(7*3)+(6*7)+(5*7)+(4*2)+(3*2)+(2*3)+(1*4)=122
122 % 10 = 2
So 37722-34-2 is a valid CAS Registry Number.

37722-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-3-hydroxy-5,5-dimethyl-cyclohex-2-enone

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:37722-34-2 SDS

37722-34-2Relevant articles and documents

A convenient and efficient preparation of β-substituted α-haloenones from diazodicarbonyl compounds

Lee, Yong Rok,Cho, Bang Sub,Kwon, Hyuk Jin

, p. 9333 - 9347 (2003)

Rhodium(II)-catalyzed reactions of cyclic diazodicarbonyl compounds with a variety of halides have been examined. With acid halides, β-acyloxy α-haloenones are produced in good yields. With benzyl halides, β-benzyloxy α-haloenones are obtained in good yie

Synthesis of novel derivatives of 7,8-dihydro-6H-imidazo[2,1-b][1,3]benzothiazol-5-one and their virus-inhibiting activity against influenza A virus

Galochkina, Anastasia V.,Bollikanda, Rakesh K.,Zarubaev, Vladimir V.,Tentler, Dmitry G.,Lavrenteva, Irina N.,Slita, Alexander V.,Chirra, Nagaraju,Kantevari, Srinivas

, (2018/12/13)

Influenza remains a highly pathogenic and hardly controlled human infection. The ability of selecting drug-resistant variants necessitates the search and development of novel anti-influenza drugs. Herein, we describe the synthesis and evaluation of a seri

A mild and regioselective method for α-bromination of β-keto esters and 1,3-diketones using bromodimethylsulfonium bromide (BDMS)

Khan, Abu T.,Ali, Md. Ashif,Goswami, Papori,Choudhury, Lokman H.

, p. 8961 - 8963 (2007/10/03)

Bromodimethylsulfonium bromide has been found to be an effective and regioselective reagent for α-monobromination of β-keto esters and 1,3-diketones. A wide variety of β-keto esters and 1,3-diketones undergo chemoselective α-monobromination with excellent yields at 0-5 °C or room temperature. The notable advantages of this protocol are no need of chromatographic separation, use of less hazardous reagent than molecular bromine, and no added base, Lewis acid, or other catalyst.

A convenient halogenation of α,β-unsaturated carbonyl compounds with OXONE and hydrohalic acid (HBr,HCl)

Kim, Kyoung-Mahn,Park, In-Hwan

, p. 2641 - 2644 (2007/10/03)

Mixtures of OXONE and hydrobromic acid or hydrochloric acid afford solutions of bromine or chlorine, respectively, α-Bromo- or α-chloro-α,β-unsaturated carbonyl compounds were prepared by addition of hydrobromic acid or hydrochloric acid to the mixture of

A new versatile route to the synthesis of novel pyrazole and fused pyrazole derivatives via intramolecular Michael reaction

El-Bermawy,Abdel Aal,El-Swah,Kadry,Al-Ashmawi

, p. 580 - 584 (2007/10/03)

Pyrazole moiety is contained in various biologically significant compounds. Therefore, we developed a synthetic route to different pyrazole derivatives which is described herein. The method shown in this work involves the utilization of active methylene c

PREPARATION AND ENOL ALLYL REARRANGEMENT OF POLYCHLORINATED DIMEDONE AND 4,4-DIMETHYL-1,3-CYCLOPENTANEDIONE DERIVATIVES

Buyck, L. De,Verhe, R.,Kimpe, N. De,Schamp, N.

, p. 307 - 322 (2007/10/02)

The 2-position in 5,5-dimethyl-1,3-cyclohexanedione (dimedone) and in 4,4-dimethyl-1,3-cyclopentanedione or their derivatives is completely and exclusively chlorinated with chlorine in dichloromethane.Dimethylformamide-hydrogen chloride mixtures, especial

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