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62018-55-7

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62018-55-7 Usage

Preparation

Obtained by reaction of acetonitrile with 2,4,6-trihydroxy-benzaldehyde (Houben-Hoesch reaction) Also obtained by reaction of ethyl orthoformate with phloracetophenone in the presence of aluminium chloride Preparation by adding successively zinc cyanide and aluminium chloride to a solution of phloracetophenone in ethyl ether. The reaction mixture was cooled in ice and saturated with hydrogen chlorideAlso obtained by reaction of DMF with phloracetophenone in the presence of phosphorous oxychloride at 20° for 1 h (70%).

Check Digit Verification of cas no

The CAS Registry Mumber 62018-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,1 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62018-55:
(7*6)+(6*2)+(5*0)+(4*1)+(3*8)+(2*5)+(1*5)=97
97 % 10 = 7
So 62018-55-7 is a valid CAS Registry Number.

62018-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-acetyl-2,4,6-trihydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-acetyl-2,4,6-trihydroxy-benzaldehyde

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:62018-55-7 SDS

62018-55-7Relevant articles and documents

The Mosaic of Rottlerin

Hong, Kenneth K. C.,Ball, Graham E.,Black, David Stc.,Kumar, Naresh

, p. 10668 - 10674 (2015/11/18)

The first total synthesis of rottlerin is described. The methodology allows the development of potential novel protein kinase C δ (PKCδ) analogues for better treatment of various diseases. Kamalachalcone A and dimeric rottlerin were synthesized in a very

Biomimetic synthesis, antimicrobial, antileishmanial and antimalarial activities of euglobals and their analogues

Bharate, Sandip B.,Bhutani, Kamlesh K.,Khan, Shabana I.,Tekwani, Babu L.,Jacob, Melissa R.,Khan, Ikhlas A.,Singh, Inder Pal

, p. 1750 - 1760 (2007/10/03)

In the present communication, naturally occurring phloroglucinol- monoterpene adducts, euglobals G1-G4 (3b/a and 4a/b) and 16 new analogues (13a/b-18a/b and 19-22) were synthesized by biomimetic approach. These synthetic compounds differ from natural euglobals in the nature of monoterpene and acyl functionality. All of these compounds were evaluated for their antibacterial, antifungal, antileishmanial and antimalarial activities. Analogue 17b possessed good antibacterial activity against methicillin-resistant Staphylococcus aureus, while analogues 19-22 possessed potent antifungal activity against Candida glabrata with IC50s ranging from 1.5 to 2.5 μg/mL. Euglobals along with all synthesized analogues exhibited antileishmanial activity. Amongst these, euglobal G2 (3a), G3 (4a) and analogues 13a and 14a showed potent antileishmanial activity with IC50s ranging from 2.8 to 3.9 μg/mL. Analogue 16a possessed antimalarial activity against chloroquine sensitive D6 clone of Plasmodium falciparum. None of the compounds showed toxicity against mammalian kidney fibroblasts (vero cells) upto the concentration of 4.76 μg/ml.

Macrocarpals, Antibacterial Compounds from Eucalyptus, Inhibit Aldose Reductase

Murata, Masatsune,Yamakoshi, Yoko,Homma, Seiichi,Arai, Koshi,Nakamura, Yoshiyuki

, p. 2062 - 2063 (2007/10/02)

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