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1706-15-6

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1706-15-6 Usage

General Description

(2-Methylnaphthalen-1-yl)Methanol, also known as 2-methyl-1-naphthyl methanol, is a chemical compound with the molecular formula C12H12O. It is a colorless to pale yellow liquid with a floral odor. (2-Methylnaphthalen-1-yl)Methanol is primarily used as an intermediate for the synthesis of perfumes, fragrances, and other aromatic compounds. It is also used in the manufacture of pharmaceuticals and as a solvent in various industrial processes. (2-Methylnaphthalen-1-yl)Methanol is considered to be a moderately toxic substance and should be handled with care in a controlled laboratory or industrial setting.

Check Digit Verification of cas no

The CAS Registry Mumber 1706-15-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1706-15:
(6*1)+(5*7)+(4*0)+(3*6)+(2*1)+(1*5)=66
66 % 10 = 6
So 1706-15-6 is a valid CAS Registry Number.

1706-15-6Relevant articles and documents

PERI-METHANOARENES BY THERMOLYSIS OF TRIMETHYLSILANES

Engler, T. A.,Shechter, H.

, p. 2715 - 2718 (1982)

Practical syntheses of varied peri-methanoarenes have been developed.

Regioselective reductive opening of substituted phthalans: synthetic applications

García, Daniel,Foubelo, Francisco,Yus, Miguel

, p. 4275 - 4286 (2008/09/20)

The reductive opening of substituted phthalans 6, 11, 12, 20, 21 and 28 with lithium and a catalytic amount of DTBB leads to the formation of corresponding functionalised organolithium intermediates 8, 15, 16, 23, 25 and 29+30 in a regioselective manner. The further reaction of these dianions with different electrophiles, mainly carbonyl compounds, gives the expected functionalised benzylic alcohols 9, 17, 18, 24, 26 and 31+32. The observed stereochemistry can be easily explained taking into account the values of the electron densities deduced by semiempirical PM3 calculations.

Facile reductive coupling of benzylic halides with ferrous oxalate dihydrate

Khurana, Jitender M.,Chauhan, Sushma,Maikap, Golak C.

, p. 1737 - 1740 (2007/10/03)

Facile reductive coupling of benzylic halides is reported with ferrous oxalate dihydrate in DMF or HMPA under nitrogen atmosphere at 155-160°C. The coupling is proposed to proceed by two successive oxidative additions of benzylic halides to ferrous oxalate to give an intermediate organoiron complex which undergoes concerted dimerization to give the corresponding reductively coupled dimers in high yields.

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