70475-59-1

Basic information

• Product Name: 5-(chlorocarbonyl)benzene-1,2,3-triyl triacetate
• Synonyms: Benzoyl chloride, 3,4,5-tris(acetyloxy)-
• CAS NO: 70475-59-1
• Molecular Formula: C₁₃H₁₁ClO₇
• Molecular Weight: 314.6752
• Mol File: 70475-59-1.mol
• Article Data: 45

Chemical Properties

• Boiling Point: 445°C at 760 mmHg
• Flash Point: 180.4°C
• Density: 1.375g/cm³
• Vapor Pressure: 4.11E-08mmHg at 25°C
• Refractive Index: 1.528
• CAS DataBase Reference: 5-(chlorocarbonyl)benzene-1,2,3-triyl triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(chlorocarbonyl)benzene-1,2,3-triyl triacetate(70475-59-1)
• EPA Substance Registry System: 5-(chlorocarbonyl)benzene-1,2,3-triyl triacetate(70475-59-1)

Safety Data

• Hazardous Substances Data: 70475-59-1(Hazardous Substances Data)

Upstream product

• 20189-90-6 3,4,5-triacetoxy-benzoic acid methyl ester 
• 149-91-7 3,4,5-trihydroxybenzoic acid 
• 6635-24-1 3,4,5-triacetoxybenzoic acid 

Downstream Products

• 112223-45-7 4-(3,4,5-triacetoxy-benzoyloxy)-coumarin 
• 104575-37-3 (1-methyl-5-nitroimidazol-2-yl)methyl 3,4,5-triacetoxybenzoate 
• 128379-13-5 3,4,5-triacetoxy-benzoic acid anilide 
• 224432-00-2 N-benzyl-3,4,5-triacetoxybenzamide 
• 70733-98-1 4-(3,4,5-trihydroxy-thiobenzoyl)-morpholine 
• 70733-97-0 4-(3,4,5-triacetoxy-thiobenzoyl)-morpholine 
• 520-31-0 tricetin 
• 65283-06-9 (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[2-phenyl-2-(3,4,5-triacetoxy-benzoylamino)-acetylamino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 64180-30-9 4-(3,4,5-triacetoxy-benzoyl)-morpholine 

Relevant articles and documents

Synthesis, biological evaluation, and docking studies of a novel sulfonamido-based gallate as pro-chondrogenic agent for the treatment of cartilage

Gallic acid (GA) and its derivatives are anti-inflammatory agents and are reported to have potent effects on Osteoarthritis (OA) treatment. Nonetheless, it is generally accepted that the therapeutic effect and biocompatibility of GA is much weaker than it

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Gallic acid hydrogen sulfide derivative and preparation method and medical application thereof

The invention discloses a gallic acid hydrogen sulfide derivative and a preparation method and medical application thereof. The general formula of the gallic acid hydrogen sulfide derivative is A-Y-X,and A is gallic acid; Y is -C (O) O-, -C (O) NH-, -C (O) OC (O)-, -C (O) NHCH2 C (O)- or is absent, and when Y is absent, the compound is A-X; X is a moiety capable of releasing hydrogen sulfide alone or in combination with A. Compared with gallic acid and existing classic non-steroidal anti-inflammatory drugs, the gallic acid hydrogen sulfide derivative has the advantages that the anti-inflammatory activity is equivalent or enhanced, the side effects of gastrointestinal tracts and cardiovascular diseases are weakened, and the gallic acid hydrogen sulfide derivative has high anti-tumor activity and good cardiovascular and neuroprotective effects.

Syntheses, Structures, and Bioactivity Evaluation of some Transition Metal Complexes with Aroylbis(N,N-diethylthioureas) Derived from Natural Compounds

Two novel benzoylthioureas derived from gallic acid, (tri-O-acetyl)galloyl-N,N-diethylthiourea HL1, and cinnamic acid, cinnamoyl-N,N-diethylthiourea HL2 have been successfully prepared and characterized by means of elemental analysis

NOVEL α-TOCOPHEROL DERIVATIVES, AND COSMETIC USES OF THE SAME

The present invention relates to a novel andalpha;-tocopherol derivative compound and cosmetic uses thereof, more specifically, a compound represented by chemical formula 1. The present invention has an antioxidant activity as a novel compound and inhibits the activity of elastase, which is a degradation enzyme of elastin protein related to wrinkle formation of skin, thereby having an effect of alleviating skin wrinkles. In the chemical formula 1, n is 3, and R_1 is each independently hydrogen, a methyl group, or an acetyl group.COPYRIGHT KIPO 2019