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3952-42-9

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3952-42-9 Usage

Uses

Different sources of media describe the Uses of 3952-42-9 differently. You can refer to the following data:
1. 9-N-Butylfluorene is used as a reagent (or an intermediate) in the synthesis of selenol esters. 9-N-Butylfluorene is also used in the prepartion of bifluorenes (e.g. T291200) via chloride-mediated radical coupling.
2. 9-N-Butylfluorene is used as a reagent (or an intermediate) in the synthesis of selenium-containing esters. 9-N-Butylfluorene is also used in the prepartion of bifluorenes (e.g. T291200) via chloride-mediated radical coupling.

Check Digit Verification of cas no

The CAS Registry Mumber 3952-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,5 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3952-42:
(6*3)+(5*9)+(4*5)+(3*2)+(2*4)+(1*2)=99
99 % 10 = 9
So 3952-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H18/c1-2-3-8-13-14-9-4-6-11-16(14)17-12-7-5-10-15(13)17/h4-7,9-13H,2-3,8H2,1H3

3952-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-butyl-9H-fluorene

1.2 Other means of identification

Product number -
Other names 9-n-butylfluorene

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:3952-42-9 SDS

3952-42-9Downstream Products

3952-42-9Relevant articles and documents

UNEXPECTED PRODUCTS IN A KABACHNIK-FIELDS SYNTHESIS OF AMINOPHOSPHONATES

Gancarz, Roman

, p. 59 - 64 (2007/10/02)

In a Kabachnik-Fields synthesis of aminophosphonates derived from aromatic ketones the formation of hydroxyphosphonates, their rearrangement to corresponding phosphates and amine promoted decomposition of the last, leads to a number of unexpected products, which in some cases could be the only products of reaction.Key words: 1-Aminophosphonates; 1-hydroxyphosphonates; Kabachnik-Fields reaction; phosphonate-phosphate rearrangement.

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