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31537-71-0

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31537-71-0 Usage

Uses

rac N-Acetyl Norlaudanosine is used in forensic analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 31537-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,3 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31537-71:
(7*3)+(6*1)+(5*5)+(4*3)+(3*7)+(2*7)+(1*1)=100
100 % 10 = 0
So 31537-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H27NO5/c1-14(24)23-9-8-16-12-21(27-4)22(28-5)13-17(16)18(23)10-15-6-7-19(25-2)20(11-15)26-3/h6-7,11-13,18H,8-10H2,1-5H3

31537-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name rac N-Acetyl Norlaudanosine

1.2 Other means of identification

Product number -
Other names 1-[1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]ethanone

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:31537-71-0 SDS

31537-71-0Downstream Products

31537-71-0Relevant articles and documents

Photochemically induced cyclization of N-[2-(o-styryl)phenylethyl]acetamides and 5-styryl-1-methyl-1,2,3,4-tetrahydroisoquinolines: New total syntheses of 1-methyl-1,2,3,4-tetrahydronaphtho[2,1-f]isoquinolines

Martínez, Elena,Estévez, Juan C,Estévez, Ramón J,Castedo, Luis

, p. 1981 - 1986 (2007/10/03)

Two new total syntheses of 1-methyl-1,2,3,4-dihydronaphtho[1,2-f]isoquinolines are based on photochemically induced cyclization of N-{2-[(E)-2-phenyl-1-etheynyl]phenylethyl]}acetamides or 1-methyl-5-[(E)-2-phenyl-1-ethenyl]-1,2,3,4-tetrahydroisoquinolines.

Illicit Heroin Manufacturing Byproducts: Copillary Gas Chromatographic Determination and Structural Elucidation of Narcotine- and Norlaudanosine-Related Compounds

Allen, Andrew C.,Cooper, Donald A.,Moore , James M.,Gloger, Manfred,Neumann, Helmut

, p. 2940 - 2947 (2007/10/02)

Capillary gas chromatographic methodology is described for detection of trace quantities of narcotine- and norlaudanosine-related manufacturing impurities in illicit heroin.N-Acetylnornarcotine (2), N-acetylanhydronornarceine (3a,b), 1-acetoxy-N-acetylanhydro-1,9-dihydronornarceine (4a,b),and (E)-3-acrylic acid(5) result from the reaction of narcotine (1) with acetic anhydride.The treatment of norlaudanosine (11a) with acetic anhydride yields N-acetylnorlaudanosine (9).After isolation from thebulk heroin matrix, these impurities, along with morphine, codeine, and thebaine byproducts, are detected by using both fused silica and glass capillary columns in the split mode with flame ionization detection.The syntheses and spectral characterization of these impurities are described.

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