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2-Amino-17-methyl-4,5α-epoxy-7,8-didehydromorphinan-3,6α-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51006-03-2

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51006-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51006-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,0 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51006-03:
(7*5)+(6*1)+(5*0)+(4*0)+(3*6)+(2*0)+(1*3)=62
62 % 10 = 2
So 51006-03-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H20N2O3/c1-19-5-4-17-9-2-3-12(20)16(17)22-15-13(17)8(7-11(9)19)6-10(18)14(15)21/h2-3,6,9,11-12,16,20-21H,4-5,7,18H2,1H3/t9-,11+,12-,16-,17-/m0/s1

51006-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,4aR,7S,7aR,12bS)-10-amino-3-methyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol

1.2 Other means of identification

Product number -
Other names Aminomorphine

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:51006-03-2 SDS

51006-03-2Downstream Products

51006-03-2Relevant academic research and scientific papers

Formation of novel thiazolomorphinans and thiazoloaporphines

Girán, Levente,Berényi, Sándor,Sipos, Attila

, p. 10388 - 10394 (2008)

A novel strategy has been developed for the synthesis of ring A fused thiazolomorphinans and ring D fused thiazoloaporphines offering the possibility of formation of regioisomeric products. The conventional thermal thiazole-forming reaction was replaced with microwave initiation and a detailed discussion has been presented on the proposed mechanism of the ring closure.

Synthesis of morphinans with diversely functionalized benzoxazole moieties

Giran, Levente,Gyulai, Zsuzsanna,Antus, Sandor,Berenyi, Sandor,Sipos, Attila

, p. 1135 - 1143 (2010)

Three independent strategies have been established for the synthesis of morphinans with oxazole moieties derived from the aminophenol function of 2-aminomorphine. All the procedures possess the ability to furnish diversely substituted 2′-oxazole moieties

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