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115552-48-2

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115552-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115552-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,5,5 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115552-48:
(8*1)+(7*1)+(6*5)+(5*5)+(4*5)+(3*2)+(2*4)+(1*8)=112
112 % 10 = 2
So 115552-48-2 is a valid CAS Registry Number.

115552-48-2SDS

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-(benzylcarbonyl)carbazole

1.2 Other means of identification

Product number -
Other names .9-Phenylacetyl-carbazol

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:115552-48-2 SDS

115552-48-2Relevant articles and documents

Iridium-PPh3 Catalysts for Conversion of Amides to Enamines

Une, Yuta,Tahara, Atsushi,Miyamoto, Yasumitsu,Sunada, Yusuke,Nagashima, Hideo

supporting information, p. 852 - 862 (2019/03/04)

Studies on the deactivation mechanism of the reaction of N,N-dialkylamides with TMDS catalyzed by Vaska's complex, IrCl(CO)(PPh3)2 (1a), triggered the discovery of highly active Ir-PPh3 catalysts: Photochemically activated

Synthesis of N-acylcarbazoles through palladium-catalyzed aryne annulation of 2-haloacetanilides

Lu, Chun,Markina, Nataliya A.,Larock, Richard C.

, p. 11153 - 11160 (2013/02/22)

N-Acylcarbazoles have been synthesized in moderate to good yields by the annulation of in situ generated arynes with 2-haloacetanilides in the presence of a palladium catalyst and CsF. Both C-C and C-N bonds are formed simultaneously, and a variety of fun

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