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Chemical structure of CAS 569-42-6

1,8-Dihydroxynaphthalene

In Stock•Starting at $10 for 250 mg•Purity ≥ 95%
CAS No.569-42-6
MDL No.MFCD00042701
MFC10H8O2
MW160.17
InChI KeyOENHRRVNRZBNNS-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
250 mg98%$10In Stock
1 g98%$21In Stock
5 g98%$71In Stock
10 g98%$109In Stock
25 g98%$259In Stock
100 g98%$743In Stock
1 kg95%+$3149In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Naphthalene-1,8-diol is a naphthalenediol in which the hydrogens at positions 1 and 8 are replaced by hydroxy groups. It functions as a fungal metabolite.

CAS No.569-42-6
Product Name1,8-Dihydroxynaphthalene
CorrosiveCorrosive
Signal Word:Danger
HCode:H318
PCode:P264+P265-P280-P305+P354+P338-P317

Related Articles

Studies related to this compound and its mechanism of action

Evidence for 1,8-dihydroxynaphthalene melanin in three halophilic black yeasts grown under saline and non-saline conditions.

FEMS microbiology letters • Vol. 232, Issue 2 • 2004
PMID: 15033240DOI: 10.1016/S0378-1097(04)00073-4

Identification of 1,8-dihydroxynaphthalene melanin in Monosporascus cannonballus and the analysis of hexaketide and pentaketide compounds produced by wild-type and pigmented isolates of the fungus.

Journal of agricultural and food chemistry • Vol. 52, Issue 13 • 2004
PMID: 15212456DOI: 10.1021/jf0308298

Efficient disruption of a polyketide synthase gene ( pks1) required for melanin synthesis through Agrobacterium-mediated transformation of Glarea lozoyensis.

Molecular genetics and genomics : MGG • Vol. 268, Issue 5 • 2003
PMID: 12589439DOI: 10.1007/s00438-002-0780-4

Biosynthesis of fungal melanins and their importance for human pathogenic fungi.

Fungal genetics and biology : FG & B • Vol. 38, Issue 2 • 2003
PMID: 12620252DOI: 10.1016/s1087-1845(02)00526-1

Documentation

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