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5,8-DIMETHYLBELLIDIFOLIN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 49599-09-9 Structure
  • Basic information

    1. Product Name: 5,8-DIMETHYLBELLIDIFOLIN
    2. Synonyms: 5,8-DIMETHYLBELLIDIFOLIN
    3. CAS NO:49599-09-9
    4. Molecular Formula: C16H14O6
    5. Molecular Weight: 302.281
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 49599-09-9.mol
  • Chemical Properties

    1. Melting Point: 204.5 °C
    2. Boiling Point: 513.5°Cat760mmHg
    3. Flash Point: 193.6°C
    4. Appearance: /
    5. Density: 1.349g/cm3
    6. Vapor Pressure: 3.62E-11mmHg at 25°C
    7. Refractive Index: 1.607
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 6.53±0.20(Predicted)
    11. CAS DataBase Reference: 5,8-DIMETHYLBELLIDIFOLIN(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5,8-DIMETHYLBELLIDIFOLIN(49599-09-9)
    13. EPA Substance Registry System: 5,8-DIMETHYLBELLIDIFOLIN(49599-09-9)
  • 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: 49599-09-9(Hazardous Substances Data)

49599-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49599-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,9 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 49599-09:
(7*4)+(6*9)+(5*5)+(4*9)+(3*9)+(2*0)+(1*9)=179
179 % 10 = 9
So 49599-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O6/c1-19-8-6-9(17)13-12(7-8)22-16-11(21-3)5-4-10(20-2)14(16)15(13)18/h4-7,17H,1-3H3

49599-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3,5,8-trimethoxyxanthen-9-one

1.2 Other means of identification

Product number -
Other names 1-hydroxy-3,5,8-trimethoxy-xanthen-9-one

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:49599-09-9 SDS

49599-09-9Downstream Products

49599-09-9Relevant articles and documents

TRI- AND TETRAOXYGENATED XANTHONES FROM SWERTIA PETIOLATA

Khetwal, Khadga S.,Joshi, Binita,Bisht, R. S.

, p. 1265 - 1267 (1990)

A new tetra-oxygenated xanthone glycoside: 1-glucosyloxy-3-hydroxy-5,8-dimethoxyxanthone has been isolated and identified from the methanolic extract of the aerial parts of Sweria petiolata along with 1,8-dihydroxy-3,5-dimethoxyxanthone; 1,3-dihydroxy-7-methoxyxanthone and 1,7-dihydroxy-3-methoxyxanthone

A XANTHONE FROM SWERTIA CHIRAYITA

Asthana, Rakesh K.,Sharma, Narendra K.,Kulshreshtha, Dinesh K.,Chatterjee, Sunil K.

, p. 1037 - 1039 (1991)

The structure of new xanthone from Swertia chirayita has been established as 1,5-dihydroxy-3,8-dimethoxy xanthone (chiratol) on the basis of spectral and chemical evidence.Two other xanthones, i. e. swerchirin (1,8-dihydroxy-3,5-dimethoxy xanthone) and 7-O-methyl swertianin (1,8-dihydroxy-3,7-dimethoxy xanthone) have been isolated.Swerchirin was identified as the hypoglycaemic principle of the plant.

Xanthone glycoside constituents of Swertia kouitchensis with α-glucosidase inhibitory activity

Wan, Luo-Sheng,Min, Qiu-Xia,Wang, Yong-Long,Yue, Yao-Dong,Chen, Jia-Chun

, p. 1248 - 1253 (2013/08/23)

Ten new xanthone glycosides, kouitchensides A-J (1-10), and 11 known analogues were isolated from an n-butanol fraction of Swertia kouitchensis. The structures of these glycosides were determined on the basis of extensive spectroscopic data interpretation and comparison with data reported in the literature. In an in vitro test, compounds 2, 4, 5, 6, 11, 12, and 13 (IC 50 values in the range 126 to 451 μM) displayed more potent inhibitory effects against α-glucosidase activity than the positive control, acarbose (IC50 value of 627 μM).

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