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"2H-Naphtho[1,2-b]pyran-5-carboxylic acid, 6-hydroxy-2,2-bis(4-methoxyphenyl)-, methyl ester" is a complex organic compound with the molecular formula C21H18O7. It is a derivative of 2H-naphtho[1,2-b]pyran-5-carboxylic acid, featuring a 6-hydroxy group and two 4-methoxyphenyl substituents at the 2-position. The methyl ester functional group is present, indicating that the carboxylic acid group has been esterified with methanol. 2H-Naphtho[1,2-b]pyran-5-carboxylic acid, 6-hydroxy-2,2-bis(4-methoxyphenyl)-, methyl ester is characterized by its unique molecular structure, which includes a naphthalene ring fused to a pyran ring, and it is likely to have specific chemical properties and potential applications in fields such as pharmaceuticals or materials science, given its intricate structure and functional groups.

169682-11-5

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169682-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169682-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,6,8 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 169682-11:
(8*1)+(7*6)+(6*9)+(5*6)+(4*8)+(3*2)+(2*1)+(1*1)=175
175 % 10 = 5
So 169682-11-5 is a valid CAS Registry Number.

169682-11-5SDS

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 methyl 6-hydroxy-2,2-bis(4-methoxyphenyl)-2H-naphtho[1,2-b]pyran-5-carboxylate

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-2,2-bis-(4-methoxy-phenyl)-2H-benzo[h]chromene-5-carboxylic acid methyl ester

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:169682-11-5 SDS

169682-11-5Relevant academic research and scientific papers

NOVEL SUBSTITUTED NAPHTHOPYRANS

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Page/Page column 15, (2010/11/08)

Described are novel reversible photochromic 2H-naphtho[1,2-b]pyran compounds, examples of which are compounds having certain substituents at the number 5 carbon atom of the naphtho-portion of the naphthopyran and at the 2-position of the pyran ring. Certain substituents may also be present at the number 6, 7, 8, 9 or 10 carbon atoms of the naphtho portion of the naphthopyran. Also described are organic host materials that contain or that are coated with such compounds. Articles such as ophthalmic lenses or other plastic transparencies that incorporate the novel naphthopyran compounds or combinations thereof with complementary photochromic compounds, e.g., spiro(indoline) type compounds, are also described.

Synthesis and photochromic properties of methoxy substituted 2,2-diaryl-2H-naphtho[1,2-b]pyrans

Gabbutt, Christopher D.,Hepworth, John D.,Heron, B. Mark,Thomas, David A.,Kilner, Colin,Partington, Steven M.

, p. 567 - 582 (2007/10/03)

A series of methoxy-substituted 2,2-di(4-methoxyphenyl)-2H-naphtho[1,2-b]pyrans has been synthesised from 3-alkoxycarbonyl-1-naphthols and 1,1-di(4-methoxyphenyl)prop-2-yn-1-ol. The influence of the methoxy group on the wavelength of maximum absorption an

Substituted naphthopyrans

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, (2008/06/13)

Described are novel reversible photochromic 2H-naphtho[1,2-b]pyran compounds, examples of which are compounds having certain substituents at the 5 and 6-positions of the naphtho portion of the naphthopyran and at the 2-position of the pyran ring, e.g., 2,2-bis(4-methoxy phenyl)-5-methoxycarbonyl-6-morpholino-2H-naphtho[1,2-b]pyran. Certain substituents may also be present at the number 7, 8, 9 or 10 carbon atoms of the naphtho portion of the naphthopyran. Also described are organic host materials that contain or that are coated with such compounds. Articles such as ophthalmic lenses or other plastic transparencies that incorporate the novel naphthopyran compounds or combinations thereof with complementary photochromic compounds, e.g., spiro(indoline) type compounds, are also described.

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