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2-chloro-5-hydroxy-3-methoxytoluene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78135-47-4 Structure
  • Basic information

    1. Product Name: 2-chloro-5-hydroxy-3-methoxytoluene
    2. Synonyms: 2-chloro-5-hydroxy-3-methoxytoluene
    3. CAS NO:78135-47-4
    4. Molecular Formula:
    5. Molecular Weight: 172.611
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78135-47-4.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: 2-chloro-5-hydroxy-3-methoxytoluene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-5-hydroxy-3-methoxytoluene(78135-47-4)
    11. EPA Substance Registry System: 2-chloro-5-hydroxy-3-methoxytoluene(78135-47-4)
  • 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: 78135-47-4(Hazardous Substances Data)

78135-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78135-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,3 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78135-47:
(7*7)+(6*8)+(5*1)+(4*3)+(3*5)+(2*4)+(1*7)=144
144 % 10 = 4
So 78135-47-4 is a valid CAS Registry Number.

78135-47-4Relevant articles and documents

Total synthesis of graphislactone G

Cudaj, Judith,Podlech, Joachim

supporting information; experimental part, p. 3092 - 3094 (2010/07/18)

We present a total synthesis of the fungal natural product graphislactone G, a chlorinated resorcylic lactone. The key step is a Suzuki coupling used for the construction of the central biaryl bond. Graphislactone G was prepared in 13 steps with 22% yield

104. Synthese de l'eriodermine

Pulgarin, Cesar,Gunziger, Jan,Tabacchi, Raffaele

, p. 945 - 948 (2007/10/02)

Synthesis of Eriodermin.The total synthesis of eriodermin (=2,7-dichloro-4-formyl 3-hydroxy-8-methoxy-1,6-dimethyl-11H-dibenzodioxepin-11-one) is described.

Depsidone Synthesis. Part 16. Benzophenone-Grisa-3',5'-diene-2',3-dione-depsidone Interconversion: a New Theory of Depsidone Biosynthesis

Sala, Tony,Sargent, Melvyn V.

, p. 855 - 869 (2007/10/02)

The synthesis of a number of grisa-3',5'-diene-2',3-diones by oxidative coupling of substituted 2,2'-dihydroxy-4-methoxybenzophenones is described.The rearrangement of these grisadienediones to depsidones under basic, acidic, and thermal conditions is des

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