527-55-9 Usage
General Description
4,5-Dimethylresorcinol is an organic chemical compound of the resorcinol family. It's scientifically identified as C8H10O2 and contains two methyl groups on its aromatic ring. This chemical is largely present in several manufacturing industries due to its diverse range of scientific and industrial applications. It is used in the production of light stabilizers in the polymer industry, as an intermediary in pharmaceuticals, and in manufacturing dyes. However, due to its reactive nature, 4,5-dimethylresorcinol should be carefully handled, as exposure could result in eye or skin irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 527-55-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 527-55:
(5*5)+(4*2)+(3*7)+(2*5)+(1*5)=69
69 % 10 = 9
So 527-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2/c1-5-3-7(9)4-8(10)6(5)2/h3-4,9-10H,1-2H3
527-55-9Relevant articles and documents
PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS
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, (2010/03/02)
The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.
Synthesis of tetra- and pentasubstituted benzenes from dimedone and derivatives
Nelson,Nelson
, p. 1287 - 1290 (2007/10/02)
Treatment of dimedone (5,5-dimethylcyclohexane-1,3-dione) and derivatives with one molar equivalent of sulfuric acid in trifluoroacetic anhydride leads, via sulfonation and a 1,2-methyl group migration, to a variety of dimethylresorcinol derivatives. The
Intermediates in the barnol biosynthesis in Penicillium baarnense
Better,Gatenbeck
, p. 391 - 394 (2007/10/12)
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