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110110-38-8

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110110-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110110-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,1 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 110110-38:
(8*1)+(7*1)+(6*0)+(5*1)+(4*1)+(3*0)+(2*3)+(1*8)=38
38 % 10 = 8
So 110110-38-8 is a valid CAS Registry Number.

110110-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-9H-carbazole-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 9H-Carbazole-1-carboxaldehyde,2-phenyl

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:110110-38-8 SDS

110110-38-8Downstream Products

110110-38-8Relevant articles and documents

Metal-free one-pot protocol for the preparation of unexpected carbazole derivative in water: Easy access to pyrimidocarbazole and pyridocarbazolone derivatives

Biswas, Soumen,Majee, Debashis,Dagar, Anuradha,Samanta, Sampak

, p. 2115 - 2120 (2014)

A novel, one-pot, metal-free-based catalytic system for the synthesis of a series of functionalized 1-methoxycarbonyl-2-aryl/alkyl-9H-carbazole derivatives has been successfully achieved in water medium by the combination of methyl 2-(3-formyl-1H-indol-2-yl)acetate with aryl/alkyl-substituted β-acroleins using DABCO (20 mol%), followed by treatment of HCl under air at heating conditions. This sequential one-pot protocol provides moderate to good yields (51-68%) of aforesaid compounds. In addition, biologically important carbazole-fused new heterocyclic scaffolds can be synthesized through our procedure. Georg Thieme Verlag Stuttgart, New York.

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