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7297-52-1

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7297-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7297-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7297-52:
(6*7)+(5*2)+(4*9)+(3*7)+(2*5)+(1*2)=121
121 % 10 = 1
So 7297-52-1 is a valid CAS Registry Number.

7297-52-1SDS

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 4-amino-4'-nitro-trans-stilbene

1.2 Other means of identification

Product number -
Other names Benzenamine, 4-[2-(4-nitrophenyl)ethenyl]-, (E)-

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:7297-52-1 SDS

7297-52-1Relevant articles and documents

Molecular probes for imaging of myelin

-

, (2018/06/18)

A molecular probe for labeling myelin includes a fluorescent trans-stilbene derivative.

Photoactivatable HNO-releasing compounds using the retro-Diels-Alder reaction

Adachi, Yusuke,Nakagawa, Hidehiko,Matsuo, Kazuya,Suzuki, Takayoshi,Miyata, Naoki

supporting information; experimental part, p. 5149 - 5151 (2009/03/11)

We synthesized hetero-Diels-Alder cycloadducts from acyl nitroso derivatives and 9,10-dimethylanthracene, to be photo-inducible HNO-releasing agents and found that introduction of conjugated nitroaromatic groups effectively enhanced the responsiveness of HNO release to UV-A irradiation; we confirmed photoinduced HNO formation by EPR and GCMS analysis. The Royal Society of Chemistry.

Synthesis of functional olefins using the Wittig-Horner reaction in different media

Durantini, Edgardo N.

, p. 4201 - 4222 (2007/10/03)

A convenient procedure for the synthesis of E-olefins bearing electron donor-acceptor groups is reported. A new diethyl N-aryl aminobenzylphosphonate (1d) was synthesized. Reactivity of Wittig-Horner reaction is compared. Expansion of the π-conjugate chain involves the reduction of N-methoxy-N-methyl amide to aldehyde by reaction with DIBAL-H.

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