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4707-50-0

  • Product Name:Divaric acid
  • Molecular Formula:C10H12O4
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Product Details

Purity:99%

High Purity Varinolic acid 4707-50-0 supply, Best Price

4707-50-0 Name

Name

Varinolic acid

Synonym

 2,4-Dihydroxy-6-propylbenzoic acid;Divaric acid;Varinolic Acid;Benzoic acid, 2,4-dihydroxy-6-propyl-

 

4707-50-0 Chemical & Physical Properties

Melting point 

169 °C (decomp)

Boiling point

385.8ºC at 760mmHg

Density

1.324g/cm3

Molecular Formula

C10H12O4

Molecular Weight

196.20000

Flash Point

 201.3ºC

PSA

77.76000

LogP

1.74850

Exact Mass

196.07400

Index of Refraction

1.606

High Purity Varinolic acid 4707-50-0 Usage

Varinolic acid is an analytical reference standard categorized as an intermediate in the phytocannabinoid biosynthetic pathway. Divarinic Acid is an antibacterial compound that strongly inhibits bacterial growth of Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa.

InChI:InChI=1/C10H12O4/c1-2-3-6-4-7(11)5-8(12)9(6)10(13)14/h4-5,11-12H,2-3H2,1H3,(H,13,14)

4707-50-0 Relevant articles

BIOENZYMATIC SYNTHESIS OF THC-v, CBV AND CBN AND THEIR USE AS THERAPEUTIC AGENTS

Ae Lim Kim ,Young Jae Yun ,Hyong Woo Choi ,Chang-Hee Hong ,Hyun Joo Shim ,*,Jeong Hwan Lee ,* andYoung-Cheon Kim

Plants 2022, 11(22), 3088

Prenyltransferase, also known as cannabigerolic acid synthase (CBGAS), produces cannabigerolic acid (CBGA) and cannabigerovarinic acid (CBGVA), which are derived from C21 and C19 precursors formed from olivetolic and divarinic acids, respectively. Biosynthesis pathway of cannabinoids. Hexanoyl-CoA and butyl-CoA are used as substrates to generate olivetolic and divarinic acid. 

4707-50-0 Process route

5-propyl-4-(piperazine-1-carbonyl)-1,3-diol

5-propyl-4-(piperazine-1-carbonyl)-1,3-diol

2,4-dihydroxy-6-propylbenzoic acid
4707-50-0

2,4-dihydroxy-6-propylbenzoic acid

Conditions
Conditions Yield
With potassium tert-butylate; In water; at 20 ℃;
 
divaricatic acid
491-62-3

divaricatic acid

2,4-dihydroxy-6-propylbenzoic acid
4707-50-0

2,4-dihydroxy-6-propylbenzoic acid

Conditions
Conditions Yield
With potassium hydroxide;
 
Multi-step reaction with 2 steps
1: 1.5 g / SO2Cl2 / diethyl ether / 24 h / Ambient temperature
2: 60 mg / H2SO4 / 0.25 h / 0 °C
With sulfuryl dichloride; sulfuric acid; In diethyl ether;
 

4707-50-0 Upstream products

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    divaricatic acid

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    491-57-6

    2-hydroxy-4-(2-hydroxy-4-methoxy-6-pentyl-benzoyloxy)-6-propyl-benzoic acid

  • 859935-20-9
    859935-20-9

    3,5-dibromo-2,4-dihydroxy-6-propyl-benzoic acid

  • 124-38-9
    124-38-9

    carbon dioxide

4707-50-0 Downstream products

  • 55382-52-0
    55382-52-0

    2,4-dihydroxy-6-n-propylbenzoic acid, methyl ester

  • 21855-51-6
    21855-51-6

    2,4-dihydroxy-6-propylbenzoic acid ethyl ester

  • 500-49-2
    500-49-2

    5-propyl-1,3-benzenediol

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