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2-Naphthalenecarboxylic acid, 6-(phenylmethoxy)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114804-76-1 Structure
  • Basic information

    1. Product Name: 2-Naphthalenecarboxylic acid, 6-(phenylmethoxy)-, methyl ester
    2. Synonyms:
    3. CAS NO:114804-76-1
    4. Molecular Formula: C19H16O3
    5. Molecular Weight: 292.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114804-76-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Naphthalenecarboxylic acid, 6-(phenylmethoxy)-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Naphthalenecarboxylic acid, 6-(phenylmethoxy)-, methyl ester(114804-76-1)
    11. EPA Substance Registry System: 2-Naphthalenecarboxylic acid, 6-(phenylmethoxy)-, methyl ester(114804-76-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 114804-76-1(Hazardous Substances Data)

114804-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114804-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114804-76:
(8*1)+(7*1)+(6*4)+(5*8)+(4*0)+(3*4)+(2*7)+(1*6)=111
111 % 10 = 1
So 114804-76-1 is a valid CAS Registry Number.

114804-76-1SDS

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-phenylmethoxynaphthalene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 6-benzyloxynaphthalene-2-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:114804-76-1 SDS

114804-76-1Relevant articles and documents

Multichromophoric cyclodextrins. 4. Light conversion by antenna effect

Jullien, Ludovic,Canceill, Josette,Valeur, Bernard,Bardez, Elisabeth,Lefèvre, Jean-Pierre,Lehn, Jean-Marie,Marchi-Artzner, Valérie,Pansu, Robert

, p. 5432 - 5442 (1996)

A water soluble β-cyclodextrin (CD-NA) bearing seven naphthoyl chromophores forms very stable 1:1 complexes with a merocyanine laser dye DCM-OH (4-(dicyanomethylene)-2-methyl-6-(p-(bis(hydroxyethyl)amino)-styryl)-4 H-pyran). The antenna effect, i.e. energ

Structure-activity relationships for vitamin D3-based aromatic a-ring analogues as hedgehog pathway inhibitors

Deberardinis, Albert M.,Madden, Daniel J.,Banerjee, Upasana,Sail, Vibhavari,Raccuia, Daniel S.,De Carlo, Daniel,Lemieux, Steven M.,Meares, Adam,Hadden, M. Kyle

, p. 3724 - 3736 (2014/05/20)

A structure-activity relationship study for a series of vitamin D3-based (VD3) analogues that incorporate aromatic A-ring mimics with varying functionality has provided key insight into scaffold features that result in potent, selective Hedgehog (Hh) pathway inhibition. Three analogue subclasses containing (1) a single substitution at the ortho or para position of the aromatic A-ring, (2) a heteroaryl or biaryl moiety, or (3) multiple substituents on the aromatic A-ring were prepared and evaluated. Aromatic A-ring mimics incorporating either single or multiple hydrophilic moieties on a six-membered ring inhibited the Hh pathway in both Hh-dependent mouse embryonic fibroblasts and cultured cancer cells (IC50 values 0.74-10 μM). Preliminary studies were conducted to probe the cellular mechanisms through which VD3 and 5, the most active analogue, inhibit Hh signaling. These studies suggested that the anti-Hh activity of VD3 is primarily attributed to the vitamin D receptor, whereas 5 affects Hh inhibition through a separate mechanism.

VITAMIN D RECEPTOR MODULATORS

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Page/Page column 26, (2008/06/13)

The present invention relates to novel, non-secosteroidal, phenyl-naphthalene compounds of Formula (I): wherein R, R1, RP, ZP, LP1, LP2 LNP, RP3, RN, and ZNP are defined herein, their prepa

NOVEL COMPOUNDS AND THEIR USE IN MEDICINE, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

-

Page/Page column 46, (2010/02/11)

The present invention relates to novel compounds of formula (I) and their pharmaceutically acceptable salts thereof, pharmaceutical compositions containing them. The present invention also relates to a process for the preparation of the above said novel compounds.

Optically active naphthalene compounds and liquid crystal materials and devices incorporating them

-

, (2008/06/13)

Optically active naphthalene compounds having the formula: STR1 in which X and Y are selected from combinations (a), (b) and (c): (a) X is C1-10 alkyl or alkoxy and Y is C4-16 optically active alkyl, (b) X is C1-10 alkyl o

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