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13924-50-0

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13924-50-0 Usage

General Description

Benzylidene 2-fluorenamine is a chemical compound with the molecular formula C20H15N. It is commonly used in the synthesis of various pharmaceuticals and organic compounds, and its structure contains a benzylidene group attached to a 2-fluorenamine moiety. BENZYLIDENE 2-FLUORENAMINE is known for its potential applications in the field of organic chemistry, particularly in the development of new drug candidates and bioactive molecules. It is important to handle this compound with caution and follow proper safety protocols, as it may pose health risks if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 13924-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,2 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13924-50:
(7*1)+(6*3)+(5*9)+(4*2)+(3*4)+(2*5)+(1*0)=100
100 % 10 = 0
So 13924-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H15N/c1-2-6-15(7-3-1)14-21-18-10-11-20-17(13-18)12-16-8-4-5-9-19(16)20/h1-11,13-14H,12H2/b21-14+

13924-50-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9H-fluoren-2-yl)-1-phenylmethanimine

1.2 Other means of identification

Product number -
Other names benzylidene-fluoren-2-yl-amine

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:13924-50-0 SDS

13924-50-0Downstream Products

13924-50-0Relevant articles and documents

Iron-Catalyzed Nitrene Transfer Reaction of 4-Hydroxystilbenes with Aryl Azides: Synthesis of Imines via C=C Bond Cleavage

Peng, Yi,Fan, Yan-Hui,Li, Si-Yuan,Li, Bin,Xue, Jing,Deng, Qing-Hai

, p. 8389 - 8394 (2019/10/16)

C=C bond breaking to access the C=N bond remains an underdeveloped area. A new protocol for C=C bond cleavage of alkenes under nonoxidative conditions to produce imines via an iron-catalyzed nitrene transfer reaction of 4-hydroxystilbenes with aryl azides is reported. The success of various sequential one-pot reactions reveals that the good compatibility of this method makes it very attractive for synthetic applications. On the basis of experimental observations, a plausible reaction mechanism is also proposed.

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