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4055-72-5

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4055-72-5 Usage

Uses

5-Allyl-1-methoxy-2,3-dihydroxybenzene is an intermediate in the synthesis of Myristicin (M884600), a naturally occurring insecticide and acaricide with possible neurotoxic effects on neuroblastoma cells.

Check Digit Verification of cas no

The CAS Registry Mumber 4055-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,5 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4055-72:
(6*4)+(5*0)+(4*5)+(3*5)+(2*7)+(1*2)=75
75 % 10 = 5
So 4055-72-5 is a valid CAS Registry Number.

4055-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-5-prop-2-enylbenzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 3-methoxy-5-allyl-1,2-benzenediol

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:4055-72-5 SDS

4055-72-5Relevant articles and documents

Ericifolin: An eugenol 5-O-galloylglucoside and other phenolics from Melaleuca ericifolia

Hussein,Hashim,El-Sharawy,Seliem,Linscheid,Lindequist,Nawwar

, p. 1464 - 1470 (2007)

Ericifolin, an eugenol 5-O-β-(6′-O-galloylglucopyranoside) possessing the naturally unknown phenolic moiety, 5-hydroxyeugenol, together with the two new phenolics, 2-O-p-hydroxybenzoyl-6-O-galloyl-(α/β)-4C1-glucopyranose and 3-methoxyellagic acid 4-O-rhamnopyranoside have been isolated from the antibacterial leaves extract of Melaleuca ericifolia. In addition, 19 known phenolics were also separated and characterized. All structures were elucidated on the basis of analysis of 1H, 13C NMR, HMQC, HMBC and FTMS spectral data.

SYNTHESIS OF ELEMICIN AND TOPICAL ANALGESIC COMPOSITIONS

-

, (2013/09/26)

The present invention is directed to the synthesis of elemicin and its isomeric form, and their use in topical analgesic formulations, including for dental and veterinary use. Various compositions include gels, films, dressings, cavity filling gels, having analgesic and/or antifungal properties.

Total synthesis of six natural products of benzodioxane neolignans

Jing, Xiao-Bi,Wang, Li,Han, Ying,Shi, Yao-Cheng,Liu, Yong-Hong,Sun, Jing

, p. 1001 - 1004 (2007/10/03)

(±)-Eusiderin E, (±)-Eusiderin F, (±)-Eusiderin K, (±)-Eusiderin J, (±)-Eusiderin M and (±)-Eusiderin G were first synthesized from pyrogallol, in which the Claisen Rearrangement was used to afford two important C6-C3 units.

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