10532-39-5

• 

• Basic information

  1. Product Name: diaporthin
  2. Synonyms: diaporthin;3-[(S)-2-Hydroxypropyl]-6-methoxy-8-hydroxyisocoumarin;(S)-8-Hydroxy-3-(2-hydroxypropyl)-6-methoxy-1H-2-benzopyran-1-one;1H-2-Benzopyran-1-one, 8-hydroxy-3-(2-hydroxypropyl)-6-methoxy-, (S)-;Isocoumarin, 8-hydroxy-3-(2-hydroxypropyl)-6-methoxy-, (+)-
  3. CAS NO:10532-39-5
  4. Molecular Formula: C13H14 O5
  5. Molecular Weight: 0
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 10532-39-5.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: diaporthin(CAS DataBase Reference)
  10. NIST Chemistry Reference: diaporthin(10532-39-5)
  11. EPA Substance Registry System: diaporthin(10532-39-5)

• 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: 10532-39-5(Hazardous Substances Data)

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  Cas No: 10532-39-5

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• (+)-8-HYDROXY-3-(2-HYDROXYPROPYL)-6-METHOXYISOCOUMARIN

  Cas No: 10532-39-5

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• Hangzhou Fandachem Co.,Ltd
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• diaporthin

  Cas No: 10532-39-5

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• Shanghai Run-Biotech Co., Ltd.
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10532-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10532-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,3 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10532-39:
(7*1)+(6*0)+(5*5)+(4*3)+(3*2)+(2*3)+(1*9)=65
65 % 10 = 5
So 10532-39-5 is a valid CAS Registry Number.

10532-39-5SDS

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	8-hydroxy-3-(2-hydroxypropyl)-6-methoxyisochromen-1-one

1.2 Other means of identification

Product number	-
Other names	Diaporthin

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:10532-39-5 SDS

10532-39-5Upstream product

• 186581-53-3 diazomethane 
• 118063-79-9 de-O-methyldiaporthin 
• 5859-68-7 [(3,5-dimethoxyphenyl)methyl]propanedioic acid diethyl ester 
• 123297-83-6 (R)-Methoxy-phenyl-acetic acid (S)-2-(6,8-dimethoxy-1-oxo-1H-isochromen-3-yl)-1-methyl-ethyl ester 
• 123406-74-6 (10S)-8-methoxyldiaporthin 
• 123297-82-5 isocoumarin 
• 123297-81-4 Trifluoro-acetic acid 5,7-dimethoxy-2-[2-(2,2,2-trifluoro-acetoxy)-propyl]-3H-inden-1-yl ester 
• 123297-77-8 2-Allyl-2-(3,5-dimethoxy-benzyl)-malonic acid diethyl ester 
• 123297-80-3 2-(2-Hydroxy-propyl)-5,7-dimethoxy-indan-1-one 
• 123297-79-0 2-Allyl-5,7-dimethoxy-indan-1-one 
• 123297-78-9 2-(3,5-Dimethoxy-benzyl)-pent-4-enoic acid 

10532-39-5Downstream Products

10532-39-5Related news

Biosynthesis of diaporthin (cas 10532-39-5) and orthosporin by Aspergillus ochraceus08/03/2019

Diaporthin and orthosporin were characterised from the fungus Aspergillus ochraceus D2306. Diaporthin was identified by high-resolution electron impact mass spectrometry and 1H and 13C NMR spectroscopy, from which new spectroscopic assignments were made. Orthosporin was also identified by mass s...detailed

10532-39-5Relevant articles and documents

Structure, Synthesis, and Stereochemistry of (+)-Orthosporin, a Phytotoxic Metabolite of Rhynchosporium Orthosporum

Ichihara, Akitami,Hashimoto, Masaaki,Hirai, Takamasa,Takeda, Ichiro,Sasamura, Yasuaki,et al.

, p. 1495 - 1498 (2007/10/02)

Structure of (+)-orthosporin, a phytotoxic metabolite isolated from Rhynchosporium orthosporum has been elucidated from spectroscopic data and chemical reaction, and the stereochemistry of (+)-orthosporin and (+)-diaporthin has been confirmed by the synth

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