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2-(1,1,3-trimethyl-3hydroxybutyl)-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106380-31-8

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106380-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106380-31-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,8 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106380-31:
(8*1)+(7*0)+(6*6)+(5*3)+(4*8)+(3*0)+(2*3)+(1*1)=98
98 % 10 = 8
So 106380-31-8 is a valid CAS Registry Number.

106380-31-8Downstream Products

106380-31-8Relevant academic research and scientific papers

Activity of oxygen-versus sulfur-containing analogs of the Flex-Het anticancer agent SHetA2

Watts, Field M.,Pouland, Tim,Bunce, Richard A.,Berlin, K. Darrell,Benbrook, Doris M.,Mashayekhi, Maryam,Bhandari, Dipendra,Zhou, Donghua

, p. 720 - 732 (2018)

Five series of chromans with urea and thiourea linkers connecting a chroman unit (ring A) and a 4-substituted benzene unit (ring B) have been prepared and evaluated relative to SHetA2 (NSC 721689) for activity against the human A2780 ovarian cancer cell l

Novel Heteroarotinoids as Potential Antagonists of Mycobacterium bovis BCG

Brown, Chad W.,Liu, Shengquan,Klucik, Jozef,Berlin, K. Darrell,Brennan, Patrick J.,Kaur, Devinder,Benbrook, Doris M.

, p. 1008 - 1017 (2004)

A series of 15 heteroarotinoids has been prepared and evaluated for activity against Mycobacterium bovis BCG with the thiourea-containing isoxyl (7) (0.5 μg/mL) as the standard. 2,2,4-Trimethyl-2H-chromen-7-yl 4-(methoxycarbonyl)benzoate (8) displayed the most significant activity (2.0-4. 0 μg/mL) in terms of the lowest concentration (μg/mL) (MIC, minimum inhibitory concentration) required to produce a 99% reduction in the number of colonies on a plate as compared to that system free of the agent at the same dilution of the culture suspension. Ethyl 4-{[N-(2,2,4,4-tetramethylchroman-6-yl)thiocarbamoyl]amino}benzoate (9) and [(1E,3Z,5E)-1-aza-4-methyl-6-(1,2,2,4-tetramethyl(1,2-dihydroquinolyl))hexa-1,3, 5-trienyl]amino}aminomethane-1-thione (10) exhibited activity at 5.0-10.0 and 10.0-20.0 μg/mL, respectively, while the other examples had MIC values of 20 μg/mL or greater. The inhibitory ability of 8 may occur via the inhibition of mycolic acid synthesis in a like manner as found with 7, but this requires further study. The heteroarotinoids are the first examples to exhibit inhibitory ability against the growth of Mycobacterium bovis BCB.

CHROMAN-SUBSTITUTED, TETRAHYDROQUINOLINE-SUBSTITUTED AND THIOCHROMAN-SUBSTITUTED HETEROAROTINOIDS AS ANTI-CANCER AGENTS

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Paragraph 0221-0222; 0241; 0298, (2020/03/09)

Chemical compounds that inhibit cancer cell growth are provided. The compounds are heteroarotinoids and derivatives thereof with oxygen, nitrogen or sulfur in chroman systems, tetrahydroquinoline systems, and tetrahydrothiochroman systems.

Chroman esters of phenols and benzoic acids having retinoid-like activity

-

, (2008/06/13)

Retinoid like activity is exhibited by compounds of the formula STR1 wherein the R 1 -R 7 groups are independently H or straight chain or branched chain lower alkyl or cycloalkyl of 1 to 6 carbons; X symbolizes an ester or thioester linkage, Y is cycloalk

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