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3-(2,6-Dichlor-phenyl)-prop-2-en-1-ol, also known as 3-(2,6-dichlorophenyl)allyl alcohol, is an organic compound with the chemical formula C9H8Cl2O. It is a colorless to pale yellow liquid with a molecular weight of 213.07 g/mol. 3-(2.6-Dichlor-phenyl)-prop-2-en-1-ol is characterized by the presence of a 2,6-dichlorophenyl group attached to an allyl alcohol moiety, which consists of a prop-2-en-1-ol (allyl alcohol) structure. It is used as an intermediate in the synthesis of various agrochemicals, particularly herbicides, due to its reactive functional groups and potential to form stable derivatives. The compound's properties, such as its reactivity and solubility, make it a valuable building block in the chemical industry for the development of new products with specific applications.

1734-76-5

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1734-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1734-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1734-76:
(6*1)+(5*7)+(4*3)+(3*4)+(2*7)+(1*6)=85
85 % 10 = 5
So 1734-76-5 is a valid CAS Registry Number.

1734-76-5Downstream Products

1734-76-5Relevant academic research and scientific papers

Catalytic asymmetric bromochlorination of aromatic allylic alcohols promoted by multifunctional Schiff base ligands

Huang, Wei-Sheng,Chen, Li,Zheng, Zhan-Jiang,Yang, Ke-Fang,Xu, Zheng,Cui, Yu-Ming,Xu, Li-Wen

, p. 7927 - 7932 (2016/08/30)

It was found that the tridentate O,N,O-type Schiff base ligand bearing suitable substituents was a highly effective promoter in the catalytic asymmetric bromochlorination reaction, in which the corresponding aromatic bromochloroalcohols with vicinal halogen-bearing stereocenters were formed with perfect regioselectivity, with moderate to excellent enantioselectivities (up to 93% ee), and with good yields and chemoselectivities.

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