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Benzenemethanol, a-ethynyl-4-(4-morpholinyl)-a-phenyl-, also known as 4-(4-morpholinyl)phenethyl-4-yn-1-benzenemethanol, is a complex organic compound with the chemical formula C20H21NO2. It is a derivative of benzenemethanol, featuring an ethynyl group (C≡CH) at the alpha position, a phenyl group (C6H5) at the alpha position, and a morpholinyl group (C4H8NO) attached to the 4-position of the phenyl ring. Benzenemethanol, a-ethynyl-4-(4-morpholinyl)-a-phenyl- is characterized by its unique molecular structure, which includes a benzene ring, an ethynyl group, a phenyl group, and a morpholinyl group, making it a versatile building block in the synthesis of various pharmaceuticals and other organic compounds.

194940-93-7

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194940-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194940-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,9,4 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 194940-93:
(8*1)+(7*9)+(6*4)+(5*9)+(4*4)+(3*0)+(2*9)+(1*3)=177
177 % 10 = 7
So 194940-93-7 is a valid CAS Registry Number.

194940-93-7SDS

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 1-phenyl-1-(4-morpholin-4-yl)phenyl-prop-2-yn-1-ol

1.2 Other means of identification

Product number -
Other names 1(4-morpholinophenyl)-1-phenylprop-2-yn-1-ol

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:194940-93-7 SDS

194940-93-7Relevant academic research and scientific papers

SUBSTITUTED NAPHTHOPYRANS

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Page/Page column 11, (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 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.

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