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[7S,(+)]-7-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole-9β-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2896-91-5

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2896-91-5 Usage

Occurrence

The leaves of Amsonia tabernaemontana yield this alkaloid.

Check Digit Verification of cas no

The CAS Registry Mumber 2896-91-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2896-91:
(6*2)+(5*8)+(4*9)+(3*6)+(2*9)+(1*1)=125
125 % 10 = 5
So 2896-91-5 is a valid CAS Registry Number.

2896-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 7-ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methano[1]azacycloundecino[5,4-b]indole-9-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:2896-91-5 SDS

2896-91-5Upstream product

2896-91-5Downstream Products

2896-91-5Relevant academic research and scientific papers

Synthesis of vinca alkaloids and related compounds part 94 [1]. Epimerization of compounds with aspidospermane and D-secoaspidospermane skeleton [section]

Kalaus, Gyoergy,Juhasz, Imre,Eles, Janos,Greiner, Istvan,Kajtar-Peredy, Maria,Brlik, Janos,Szabo, Lajos,Szantay, Csaba

, p. 245 - 251 (2007/10/03)

The individual epimerization steps of vincadifformine (1), deethylvincadifformine isomers (2,3), their synthetic intermediates (4-13) as well as that of simpler compounds with D-secoaspidospermane skeleton (1517) were studied a) in protic medium (boiling deuteroacetic acidic) and b) under reductive (with sodium borodeuteride in boiling acetic acid, or with sodium borohydride in boiling deuteroacetic acid) conditions.

TOTAL SYNTHESES OF EBURNAMONINE, QUEBRACHAMINE, VINCADINE AND EPIVINCADINE

Wenkert, Ernest,Halls, Timothy D. J.,Kwart, Lawrence D.,Magnusson, Goeran,Showalter, H. D. Hollis

, p. 4017 - 4025 (2007/10/02)

Syntheses of the alkaloids eburnamonine and quebrachamine are presented in which the non-tryptamine portion of the skeleta is constructed by the β-oxycyclopropylcarboxylate preparation-fragmentation route.A similar reaction scheme is utilized for the synthesis of the alkaloids vincadine and epivincadine.

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