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N,N,4′-TRIMETHYL-4-STILBENAMINE
Cas No: 7378-54-3
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Bluecrystal chem-union
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N,N,4′-TRIMETHYL-4-STILBENAMINE
Cas No: 7378-54-3
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Antimex Chemical Limied
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Benzenamine, N,N-dimethyl-4-[2-(4-methylphenyl)ethenyl]-
Cas No: 7378-54-3
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SAGECHEM LIMITED
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N,N,4′-TRIMETHYL-4-STILBENAMINE
Cas No: 7378-54-3
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Hubei Jiutian Bio-medical Technology Co., Ltd
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7378-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7378-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7378-54:
(6*7)+(5*3)+(4*7)+(3*8)+(2*5)+(1*4)=123
123 % 10 = 3
So 7378-54-3 is a valid CAS Registry Number.

InChI:InChI=1/C17H19N/c1-14-4-6-15(7-5-14)8-9-16-10-12-17(13-11-16)18(2)3/h4-13H,1-3H3

7378-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	Me2NSBMe

1.2 Other means of identification

Product number	-
Other names	4-N,N-dimethylamino-4'-methylstilbene

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:7378-54-3 SDS

7378-54-3Upstream product

7378-54-3Downstream Products

1608492-57-4 4,4'-((2R,3S,4R,5S)-3,4-di-p-tolyltetrahydrofuran-2,5-diyl)bis(N,N-dimethylaniline)

7378-54-3Relevant articles and documents

Substituent effect on the UV spectra of p-disubstituted compounds XPh(CH=CHPh)nY (n=0, 1, 2)

Chen, Guanfan,Cao, Chenzhong

scheme or table, p. 776 - 782 (2011/05/05)

Three parameters, θCCex, θ CCex(XY) and Vmax,parent, are developed to express the substituent effect and the effect of the parent molecular structure of p-disubstituted compounds XPh(CH=CHPh)nY (n=0, 1, 2). The investigated result shows a good correlation between the UV absorption wavenumbers (Vmax) and the three parameters for a diverse set of title compounds, and the correlation equation can be used to predict the UV absorption energy of compounds with the mentioned structure. This approach provides a new insight for the quantitative structure-property relationship (QSPR) correlation of the UV absorption energy of p-disubstituted homologues. Copyright

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7378-54-3