3568-90-9 Usage
Description
Deoxylapachol, the main allergen found in teak (Tectona grandis), is a compound that can cause sensitization and allergic reactions, particularly among individuals involved in woodwork and those who frequently come into contact with teak wood.
Uses
Used in Woodworking Industry:
Deoxylapachol is used as an allergen in the woodworking industry, specifically associated with teak wood (Tectona grandis). It is important for workers in this industry to be aware of the potential sensitization and allergic reactions that may occur due to exposure to deoxylapachol.
Used in Allergen Research:
Deoxylapachol is used as a subject of study in allergen research to better understand its effects on human health and to develop strategies for minimizing sensitization and allergic reactions among those exposed to it, such as woodworkers and individuals working with teak wood.
Used in Occupational Health and Safety:
Deoxylapachol is used as a reference allergen in occupational health and safety guidelines and regulations, helping to establish safety measures and protocols for workers who may come into contact with teak wood and are at risk of sensitization or allergic reactions.
Contact allergens
Deoxylapachol is the main allergen identified in teak (Tectona grandis). Sensitization often concerns people involved in woodwork.
Check Digit Verification of cas no
The CAS Registry Mumber 3568-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3568-90:
(6*3)+(5*5)+(4*6)+(3*8)+(2*9)+(1*0)=109
109 % 10 = 9
So 3568-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O2/c1-10(2)7-8-11-9-14(16)12-5-3-4-6-13(12)15(11)17/h3-7,9H,8H2,1-2H3
3568-90-9Relevant articles and documents
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Burnett,A.R.,Thomson,R.H.
, p. 850 - 853 (1968)
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Direct allylation of quinones with allylboronates
Deng, Hong-Ping,Wang, Dong,Szabó, Kálmán J.
, p. 3343 - 3348 (2015/03/30)
Allylboronates undergo C-H allylation of unsubstituted or monosubstituted benzoquinone and naphthoquinone substrates. In the case of 2,5-or 2,6-disubstituted quinones addition involving the substituted carbon takes place. Allylation with stereodefined allylboronates occurs with retention of the configuration.
Synthesis of mollugin
Claessens, Sven,Kesteleyn, Bart,Nguyen Van, Tuyen,De Kimpe, Norbert
, p. 8419 - 8424 (2007/10/03)
The total synthesis of mollugin, a major constituent of rubiaceous herbs, using a straightforward synthetic approach starting from 1,4-naphthoquinone via a sequence of reactions, including selective prenylation, epoxidation, reduction of the quinone moiety, acid-catalysed ring expansion, bromination, dehydration and methoxycarbonylation is presented.