113428-99-2

• 

• Basic information

  1. Product Name: Benzoic acid, 2-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]-
  2. Synonyms:
  3. CAS NO:113428-99-2
  4. Molecular Formula: C15H12O4
  5. Molecular Weight: 256.258
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 113428-99-2.mol
  9. Article Data: 4

• 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: Benzoic acid, 2-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Benzoic acid, 2-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]-(113428-99-2)
  11. EPA Substance Registry System: Benzoic acid, 2-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]-(113428-99-2)

• 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: 113428-99-2(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• Benzoic acid, 2-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]-

  Cas No: 113428-99-2

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113428-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113428-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,2 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113428-99:
(8*1)+(7*1)+(6*3)+(5*4)+(4*2)+(3*8)+(2*9)+(1*9)=112
112 % 10 = 2
So 113428-99-2 is a valid CAS Registry Number.

113428-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]benzoic acid

1.2 Other means of identification

Product number	-
Other names	Hydrangeaic acid

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:113428-99-2 SDS

113428-99-2Upstream product

• 507480-02-6 5-(bromomethyl)-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 438187-08-7 2, 2, 5-trimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 567-61-3 2-hydroxy-6-methylbenzoic acid 
• 480-47-7 hydrangenol 
• 13506-76-8 2-methyl-6-nitrobenzoic acid 

113428-99-2Downstream Products

• 52528-89-9 3,4'-bis-benzoyloxy-bibenzyl 
• 480-47-7 hydrangenol 
• 157598-00-0 (+/-)-hydromacrophyllol B 
• 157598-00-0 (+/-)-hydromacrophyllol A 
• 113345-84-9 methyl 2-methoxy-6-[2-(4-methoxyphenyl)ethenyl]benzoate 
• 23255-59-6 lunularic acid 
• 37116-80-6 lunularin 
• 63877-76-9 (E)-4-<2-(3-hydroxyphenyl)ethenyl>phenol 
• 183619-44-5 8-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-isochroman-1-one 
• 183619-48-9 8-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-isochromen-1-one 
• 80458-94-2 3'-Deoxythunberginol A 

113428-99-2Relevant articles and documents

-

Asahina,Asano

, (1930)

-

Compositions containing hypotriglyceridemically active stilbenoids

-

, (2008/06/13)

The use of isolated or purified stilbenoid compounds including longistyline A-2-carboxylic acid as a dietary supplement to mammals suffering from elevated triglyceride levels is described. The invention also relates to the use of such stibenoid compounds in combination with other hypotriglyceridemic agents.

Chemical transformation from dihydroisocoumarin into benzylidene-phthalide by use of regiospecific oxidative lactonization mediated by copper chloride (H) - Syntheses of thunberginol F and hydramacrophyllol A and B

Yoshikawa,Harada,Yagi,Okuno,Muraoka,Koyama,Murakami

, p. 721 - 723 (2007/10/02)

Oxidative lactonization of 2-carboxystilbene mediated by CuCl2 proceeded regiospecifically to give the five-membered lactone. By utilizing this lactonization as a key reaction, chemical transformation from dihydroisocoumarine into benzylideneph

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