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Cyclopent[b]indole-7-carboxaldehyde, 1,2,3,3a,4,8b-hexahydro-4-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

273220-35-2

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273220-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 273220-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,3,2,2 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 273220-35:
(8*2)+(7*7)+(6*3)+(5*2)+(4*2)+(3*0)+(2*3)+(1*5)=112
112 % 10 = 2
So 273220-35-2 is a valid CAS Registry Number.

273220-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-Methylphenyl)-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole-7-c arbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:273220-35-2 SDS

273220-35-2Relevant academic research and scientific papers

Aromatic pyridazine compound as well as preparation method and application thereof (by machine translation)

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Paragraph 0136-0138; 0141-0142, (2020/07/29)

The invention discloses an aromatic pyridazine compound and a use thereof. 1 H-NMR and the like are characterized in that the compound has a longer charge-off-state life and can be used as a better photoelectric material. In addition, the invention further provides a preparation method of the aromatic pyridazine compound, and the preparation method is environment-friendly and convenient to operate. The method comprises the following steps: Step 1, reacting 2 and 4 - dibromonitrobenzene as raw materials through coupling reaction, 5, 5 - dibromo -2, 2 ’ -dinitrobiphenyl, step 2 and taking R1 The substituted ethylene derivatives and 5, 5 - dibromo -2 and 2 ’ -dinitrobiphenyl serve as raw materials to synthesize nitro-substituted compounds through coupling reaction; step 3: synthesizing an aromatic pyridazine compound by a reduction reaction with the nitro-substituted compound as a raw material. The invention further discloses application of the aromatic pyridazine compound in a solar cell and application of the aromatic pyridazine compound in pH detection. (by machine translation)

Synthesis and characterization of triphenylamine modified azobenzene dyes

Zhao, Chuanwu,Wang, Tianyang,Li, Dongmei,Lu, Ting,Liu, Dongzhi,Meng, Qingbo,Zhang, Qianqian,Li, Fengqing,Li, Wei,Hu, Wenping,Wang, Lichang,Zhou, Xueqin

, p. 256 - 264 (2016/11/09)

A series of triphenylamine modified azobenzenes were synthesized and studied theoretically and experimentally. D-A-D structures of these dyes were revealed with an intramolecular charge transfer (ICT) from both triphenylamine or indoline units (donor) to

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