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63619-61-4

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63619-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63619-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,1 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63619-61:
(7*6)+(6*3)+(5*6)+(4*1)+(3*9)+(2*6)+(1*1)=134
134 % 10 = 4
So 63619-61-4 is a valid CAS Registry Number.

63619-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(n-octyl)-4'-bromobiphenyl

1.2 Other means of identification

Product number -
Other names 4-BROMO-4'-N-OCTYL-1,1'-BIPHENYL

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:63619-61-4 SDS

63619-61-4Downstream Products

63619-61-4Relevant articles and documents

Enantiotropic nematics from cross-like 1,2,4,5-tetrakis(4'-alkyl-4- ethynylbiphenyl)benzenes and their biaxiality studies

Chen, Hsiu-Hui,Lin, Hsing-An,Lai, Yin-Hui,Lin, Shu-Yu,Chiang, Chien-Hung,Hsu, Hsiu-Fu,Shih, Tzenge-Lien,Lee, Jey-Jau,Lai, Chien-Chen,Kuo, Ting-Shen

scheme or table, p. 9543 - 9551 (2012/09/07)

The theoretically predicted optimum length/breadth/width ratio for maximizing shape biaxiality was investigated experimentally by the facile and successful synthesis of cross-shaped compound 3, which showed enantiomeric nematic phase behavior. This cross-like core structure could alternatively be viewed as two fused V-shaped mesogens, which have recently immerged as a new direction in biaxial nematic research, at the bending tips that can act as a new structure for biaxial investigations. Whilst the thermal analysis data of compound 3 did not meet the expected theoretical values for biaxial nematics, surface-induced biaxiality was evidenced by optical studies. Cluster-size analysis within the nematic phase of compound 3 revealed the formation of meta-cybotactic nematics, which approached the cluster sizes of cybotactic nematics. The split small-angle 2D X-ray diffraction patterns of magnetic-field-aligned samples indicated that the nematic phase was composed of small smectic C-like clusters with the tilting of molecules within the clusters. The wide-temperature-range enantiomeric nematic phase of cross-like compound 3 enabled the molecular skeleton to serve as an alternative skeleton to bent-rod mesogens, which exhibited nematic phases with the potential competition of transitions to higher-order liquid-crystalline phases and crystallization, for future biaxial investigations. Take up your cross: An enantiotropic nematic phase with a wide temperature range has been achieved by using cross-like mesogens. Biaxiality investigations by using conoscopic and 2D XRD studies imply the formation of small smectic C-like meta-cybotactic clusters in the nematic arrangement. Copyright

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