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Benzyl alcohol, 3,4-dihydroxy-α-[(isopropylamino)methyl]-, sulfate (2:1) (salt), (+)- (8CI) is a complex organic compound with the chemical formula C16H25NO4. It is a derivative of benzyl alcohol, featuring a 3,4-dihydroxyphenyl group and an isopropylaminomethyl substituent. Benzyl alcohol, 3,4-dihydroxy-a-[(isopropylamino)methyl]-, sulfate (2:1) (salt), (+)- (8CI) is a salt formed by the reaction of the parent alcohol with sulfuric acid in a 2:1 ratio, resulting in the formation of sulfate ester groups. The (+)- notation indicates that it is the levorotatory enantiomer, which means it rotates plane-polarized light in a counterclockwise direction. Benzyl alcohol, 3,4-dihydroxy-a-[(isopropylamino)methyl]-, sulfate (2:1) (salt), (+)- (8CI) is of interest in the field of organic chemistry and pharmaceuticals, potentially serving as an intermediate in the synthesis of various drugs or as a chiral auxiliary in asymmetric synthesis.

6779-80-2

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6779-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6779-80-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,7 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6779-80:
(6*6)+(5*7)+(4*7)+(3*9)+(2*8)+(1*0)=142
142 % 10 = 2
So 6779-80-2 is a valid CAS Registry Number.

6779-80-2Relevant academic research and scientific papers

Method for preparing isoproterenol sulfate dihydrate

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Paragraph 0021, (2017/09/01)

The invention relates to a method for preparing isoproterenol sulfate dihydrate. The method comprises the following steps: (1) preparation of 2-bromo-1-(3, 4-dihydroxy phenyl)-ethanone; (2) preparation of isoproterenol ketone hydrochloride; and (3) preparation of isoproterenol sulfate dihydrate. The method disclosed by the invention adopts a reaction system of bromoacetyl bromide and aluminium chloride instead of a reaction system of monochloro acetic acid and phosphorus oxychloride, so that the method has the advantages that the environmental protection cost is reduced; the reaction yield is increased; the industrial production is benefited; the reaction condition is mild; the catalyst quantity is little; and the process is simple. Compared with conventional synthetic processes, the method disclosed by the invention has obvious economic benefit and environmental benefit.

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