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Neopine, also known as 2-(2-methoxyphenyl)-1-(1-phenylethyl)-1,3-dioxolane, is a synthetic chemical compound that belongs to the class of opioids. It is structurally similar to morphine and has been studied for its potential analgesic properties. Neopine is not approved for medical use and is not commercially available. Its chemical structure consists of a dioxolane ring with a phenylethyl group and a methoxyphenyl group attached to it. Due to its structural resemblance to morphine, neopine has been of interest in scientific research to understand the structure-activity relationships of opioids and to develop new pain management medications. However, it is important to note that neopine's safety, efficacy, and potential side effects have not been thoroughly evaluated in clinical settings.

467-14-1

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467-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 467-14-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 467-14:
(5*4)+(4*6)+(3*7)+(2*1)+(1*4)=71
71 % 10 = 1
So 467-14-1 is a valid CAS Registry Number.

467-14-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5alpha,6alpha)-8,14-Didehydro-4,5-epoxy-3-methoxy-17-methylmorphinan-6-ol

1.2 Other means of identification

Product number -
Other names Morphinan-6-ol, 8,14-didehydro-4,5-epoxy-3-methoxy-17-methyl-, (5α,6α)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:467-14-1 SDS

467-14-1Relevant academic research and scientific papers

Synthesis of neopine and its 5β- and 7-substituted derivatives (chemistry of opium alkaloids, part XL)

Meuzelaar, G. J.,Woudenberg, R. H.,Sinnema, A.,Maat, L.

, p. 573 - 577 (1993)

Heating 14β-bromocodeine (3) with methanol and triethylamine yielded 6α,7α-epoxy-6-deoxyneopine (5).The epoxide 5 was reduced to neopine (7) with lithium aluminium hydride, whereas reaction of 5 with sodium methoxide gave 7β-methoxyneopine (9).Similar reactions were performed with 14β-bromo-5β-methylcodeine (4), yielding the corresponding 5β-methyl derivatives 6, 8 and 10.Acetylation of 3 and 4 gave 6α-O-acetyl-14β-bromocodeine (11) and its 5β-methyl analogue 12, respectively, from which the ortho esters 13 and 14 were obtained after treatment with methanol.Acid hydrolysis of 13 or, better, solvolysis of 11 in water yielded a mixture of 6α-O-acetyl-7α-hydroxyneopine (15) and 7α-acetoxyneopine (17).Under the same conditions 12 and 14 gave the 5β-methyl analogues 16 and 18.

BIOTRANSFORMATION OF THEBAINE BY CELL SUSPENSION CULTURES OF PAPAVER SOMNIFERUM CV. MARIANNE

Tam, W. H. John,Kurz, Wolfgang G. W.,Constabel, Friedrich,Chatson, Kenneth B.

, p. 253 - 255 (1982)

Thebaine is biotransformed to neopine by cell suspension cultures of Papaver somniferum cv.Marianne grown in O-B5 medium.Results of precursor studies on these cell suspension cultures are also described.Key Word Index - Papaver somniferum; Papaveraceae; cell suspension culture; biotransformation; thebaine; neopine; morphinan alkaloids.

Compositions and Methods For Making Alkaloid Morphinans

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Paragraph 0051; 0236-0238, (2017/09/30)

Methods that may be used for the manufacture of a class of chemical compounds known as morphinans, including neopine, are provided. Compositions useful for the synthesis of morphinans, including neopine, are also provided.

METHOD FOR THE CATALYTIC PRODUCTION OF HYDROCODONE AND HYDROMORPHONE

-

Page/Page column 7, (2008/06/13)

A method for the catalytic conversion of codeine, morphine or analogs thereof into hydrocodone, hydromorphone or analogs thereof utilizing a transition metal complex of a tertiary phosphine halide as catalyst.

NEODIHYDROTHEBAINE AND BRACTAZONINE, TWO DIBENZAZONINE ALKALOIDS OF PAPAVER BRACTEATUM

Theuns, Hubert G.,Lenting, Herman B. M.,Salemink, Cornelis A.,Tanaka, Hitoshi,Shibata, Masayoshi,et al.

, p. 1157 - 1166 (2007/10/02)

Two new dibenzazonine alkaloids, neodihydrothebaine and bractazonine were isolated from Papaver bracteatum.Their possible biosynthesis from thebaine is discussed.The structures of both new alkaloids are proven by synthesis.An isomeric dibenzazonine compound was also prepared. - Keywords: Papaver bracteatum; Papaveraceae; alkaloids; dibenzazonines; neodihydrothebaine; bractazonine; biosynthetic pathway; synthesis; 5,6,8,9-tetrahydro-2-methoxy-7-methyl-dibenzazonin-1,12-diol; 5,6,8,9-tetrahydro-2,10-dimethoxy-7-methyl-dibenzazonin-1-ol; 5,6,8,9-tetrahydro-2,11-dimethoxy-7-methyl-dibenz-azonin-1-ol; 5,6,8,9-tetrahydro-2,12-dimethoxy-7-methyl-dibenzazonin-1-ol.

Conversions of tosyl and mesyl derivatives of the morphine group, XX. Synthesis of mesyl esters

Makleit,Berenyi,Bognar,Elek

, p. 161 - 163 (2007/10/10)

A simple and convenient method had been developed for the preparation of dihydro derivatives of morphine alkaloids. In this was, 3-O-ethyldihydromorphine was obtained in crystalline form. This compound is described in the literature as an oily product. Several 6-O-mesyl derivatives have been synthesized in good yields also on a larger scale from the dihydro compounds by the use of Crossland's method.

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