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7336-40-5

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7336-40-5 Usage

Description

A colchicine type alkaloid, N-acetyldemecolcine occurs in both the corms and seeds of Colchicum autumnale, Gloriosa virescens and Littoria modesta. It is separated from the numerous other accompanying bases by column and thin_x0002_layer chromatography. The base is laevorotatory with a specific rotation of [α]D - 2440 (c 1.0, CHC13).

Check Digit Verification of cas no

The CAS Registry Mumber 7336-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7336-40:
(6*7)+(5*3)+(4*3)+(3*6)+(2*4)+(1*0)=95
95 % 10 = 5
So 7336-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C23H27NO6/c1-13(25)24(2)17-9-7-14-11-20(28-4)22(29-5)23(30-6)21(14)15-8-10-19(27-3)18(26)12-16(15)17/h8,10-12,17H,7,9H2,1-6H3/t17-/m0/s1

7336-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-[(7S)-1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide

1.2 Other means of identification

Product number -
Other names N-Methylcolchicine

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:7336-40-5 SDS

7336-40-5Downstream Products

7336-40-5Relevant articles and documents

Biosynthesis. Part 26. Synthetic Studies of Structural Modification of Late Biosynthetic Precursors for Colchicine

Battersby, Alan R.,McDonald, Edward,Stachulski, Andrew V.

, p. 3053 - 3064 (2007/10/02)

The latter part of the natural pathway to colchicine is known to involve conversion of phenethyltetrahydroisoquinoline (2) by phenol oxidation into a dienone (O-methylandrocymbine) (4), the dienone subsequently undergoing ring-expansion to generate the tr

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