Isosalvianolic acid C

Modify Date: 2025-08-25 18:20:51

Isosalvianolic acid C Structure
Isosalvianolic acid C structure
Common Name Isosalvianolic acid C
CAS Number 142115-17-1 Molecular Weight 492.43100
Density N/A Boiling Point 853.8±65.0 °C at 760 mmHg
Molecular Formula C26H20O10 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Isosalvianolic acid C


Isosalvianolic acid C is a phenolic compound that can be found in Lavandula angustifolia Mill.. Isosalvianolic acid C can be used as antioxidant[1].

 Names

Name Isosalvianolic acid C
Synonym More Synonyms

 Isosalvianolic acid C Biological Activity

Description Isosalvianolic acid C is a phenolic compound that can be found in Lavandula angustifolia Mill.. Isosalvianolic acid C can be used as antioxidant[1].
Related Catalog
References

[1]. Nigary Yadikar, et al. Seven new phenolic compounds from Lavandula angustifolia. Phytochemistry Letters. 2018, 23: 149-154.

 Chemical & Physical Properties

Boiling Point 853.8±65.0 °C at 760 mmHg
Molecular Formula C26H20O10
Molecular Weight 492.43100
Exact Mass 492.10600
PSA 173.98000
LogP 3.74300
InChIKey AVGRZVZQTALJJF-VURDRKPISA-N
SMILES O=C(C=Cc1ccc(O)c2c1C=Cc1cc(O)c(O)cc1O2)OC(Cc1ccc(O)c(O)c1)C(=O)O

 Synonyms

(E)-3-(4,7,8-Trihydroxy-dibenzo[b,f]oxepin-1-yl)-acrylic acid (R)-1-carboxy-2-(3,4-dihydroxy-phenyl)-ethyl ester
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here



Get all suppliers and price by the below link:

Isosalvianolic acid C suppliers

Isosalvianolic acid C price

Related Compounds: More...
Isosalvianolic acid B
930573-88-9
dillenic acid C
159359-64-5
Myriceric acid C
162059-94-1
Carbonic acid,C,C'-(sulfonyldi-2,1-ethanediyl) C,C'-bis(2,5-dioxo-1-pyrrolidinyl) ester
57683-72-4
griseolic acid C
100242-49-7
1,4-Phenylene Di-Tert-Butyl Bis(Carbonate)
127175-62-6
Carbonic acid,C,C'-1,2-ethanediyl C,C'-dimethyl ester
88754-66-9
fasciculic acid C
126882-56-2
pyrenochaetic acid C
79214-47-4
1-[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-3-hydroxypyrrolidine-3-carboxylic acid
2171429-36-8
4-[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]hexanoic acid
2171443-52-8
(1RS,3RS)-3-[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]cyclohexane-1-carboxylic acid
2227760-89-4
3-{[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]methyl}oxolane-2-carboxylic acid
2171440-24-5
(2RS,3SR)-3-[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]oxolane-2-carboxylic acid
2227643-86-7
1-[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-5-hydroxypiperidine-3-carboxylic acid
2171351-54-3
2-{2-[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]cyclopentyl}acetic acid
2171333-69-8
3-{2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]butanamido}-2,2,4-trimethylpentanoic acid
2172229-53-5
3-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylbutanamido]-2,2,4-trimethylpentanoic acid
2171973-55-8
3-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanamido]-2,2,4-trimethylpentanoic acid
2172541-15-8