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2-(acetylamino)-9H-fluoren-3-yl acetate is a complex organic compound with the chemical formula C19H17NO3. It is a derivative of fluorene, a polycyclic aromatic hydrocarbon, and features an acetylamino group at the 2-position and an acetate group at the 3-position. 2-(acetylamino)-9H-fluoren-3-yl acetate is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is typically used as an intermediate in chemical reactions, particularly in the preparation of fluorene-based compounds with diverse functional groups. The compound's properties, such as its solubility and stability, can be influenced by the presence of these functional groups, making it a valuable building block in organic synthesis.

7213-98-1

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7213-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7213-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7213-98:
(6*7)+(5*2)+(4*1)+(3*3)+(2*9)+(1*8)=91
91 % 10 = 1
So 7213-98-1 is a valid CAS Registry Number.

7213-98-1SDS

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 (2-acetamido-9H-fluoren-3-yl) acetate

1.2 Other means of identification

Product number -
Other names acetamide,N-[3-(acetyloxy)-9H-fluoren-2-yl]

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 -
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More Details:7213-98-1 SDS

7213-98-1Downstream Products

7213-98-1Relevant academic research and scientific papers

The Solvolysis of N-Acetoxy-2-acetylaminofluorene and N-Acetoxy-4-acetylaminobiphenyl: Delicate Balance between Nitrenium Ion Formation and Hydrolysis

Underwood, Graham R.,Kirsch, Robert B.

, p. 136 - 138 (2007/10/02)

The solvolysis of N-acetoxy-2-acetylaminofluorene in aqueous acetone at neutral pH proceeds exclusively with nitrenium ion formation while under the same conditions, the 4-aminobiphenyl analogue undergoes exclusive acyl-oxygen scission.

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