Cas 1227191-83-4,3-butoxybenzenthiol

1227191-83-4

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Product Name: 3-butoxybenzenthiol
Synonyms: 3-butoxybenzenthiol
CAS NO:1227191-83-4
Molecular Formula:
Molecular Weight: 182.287
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-butoxybenzenthiol(CAS DataBase Reference)
NIST Chemistry Reference: 3-butoxybenzenthiol(1227191-83-4)
EPA Substance Registry System: 3-butoxybenzenthiol(1227191-83-4)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1227191-83-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1227191-83-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,1,9 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1227191-83:
(9*1)+(8*2)+(7*2)+(6*7)+(5*1)+(4*9)+(3*1)+(2*8)+(1*3)=144
144 % 10 = 4
So 1227191-83-4 is a valid CAS Registry Number.

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1227191-83-4Relevant academic research and scientific papers

Discotic liquid crystals of transition metal complexes, 53?: Synthesis and mesomorphism of phthalocyanines substituted by m -alkoxyphenylthio groups

Chino, Yoshiaki,Ohta, Kazuchika,Kimura, Mutsumi,Yasutake, Mikio

, p. 159 - 178 (2017/07/11)

We have successfully synthesized a series of novel octakis(m-alkoxyphenylthio)phthalocyaninato copper(II) complexes, (m-CnOPhS)8PcCu (n = 2, 4, 6, 8, 10, 12, 14, 16: 1b～1i), by our developed method to reveal their mesomorphism. The phase transition behavior and mesophase structures have been established by using a polarizing optical microscope, a differential scanning calorimeter, and a temperature-dependent small angle X-ray diffractometer. Interestingly, the very short chain-substituted derivatives, (m-C1OPhS)8PcCu (1a) and (m-C2OPhS)8PCu (1b), show a hexagonal ordered columnar (Colho) mesophase, whereas each of the other longer-chain-substituted derivatives, (m-CnOPhS)8PcCu (n = 4～16: 1c～1i), shows only rectangular ordered columnar (Colro) mesophase(s). In contrast to the present longer-chain-substituted phenylthio derivatives, each of the previous longer-chain-substituted phenoxy derivatives, (m-CnOPhO)8PcCu (n = 10-20), shows a different columnar mesophase of Colho. We discuss this difference of mesomorphism from the viewpoint of the different steric hindrance originated by the peripheral substituents, PhO and PhS groups. Moreover, we could estimate the optical band gaps of (m-C10OPhO)8PcCu and (m-C10OPhS)8PcCu (1f) from absorption edge of the Q-bands to be 1.79 eV and 1.70 eV, respectively. Therefore, the phenylthio-substituted derivative gave a narrower band gap byca. 0.1 eV in comparison with the phenoxy-substituted derivative.

THIOCHROMENE DERIVATIVES AS HIP HYDROXYLASE INHIBITORS

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Page/Page column 72, (2010/06/15)

The present invention relates to novel compounds, methods, and compositions capable of decreasing HEF hydroxylase enzyme activity, thereby increasing the stability and/or activity of hypoxia inducible factor (HIF).

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