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1055-75-0

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1055-75-0 Usage

Description

An Alstonia alkaloid, this base occurs in the bark of A. venenata R. Br. and has[α]24D - 76.07°. The hydriodide has m.p. 255-7°C (dec.); the picrate, m.p. 243° (dec.); the methiodide, m.p. 285-2900 C (dec.) and the O-acetate, m.p. 98-101°C (dec.). A methoxyl group, a non-phenolic hydroxyl group and a methoxycarbonyl group are present.

References

Govindachari et al., Tetrahedron Lett., 901 (1964)

Check Digit Verification of cas no

The CAS Registry Mumber 1055-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1055-75:
(6*1)+(5*0)+(4*5)+(3*5)+(2*7)+(1*5)=60
60 % 10 = 0
So 1055-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H28N2O4/c1-27-18-5-3-4-15-19(18)13-8-9-24-11-12-6-7-17(25)20(22(26)28-2)14(12)10-16(24)21(13)23-15/h3-5,12,14,16-17,20,23,25H,6-11H2,1-2H3

1055-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Venenatine

1.2 Other means of identification

Product number -
Other names 17-hydroxy-9-methoxy-yohimbane-16-carboxylic acid methyl ester

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:1055-75-0 SDS

1055-75-0Downstream Products

1055-75-0Related news

Stereochemistry and relative stability of the oxindoles derived from venenatine (cas 1055-75-0) and alstovenine. the two c-3 epimeric 9-methoxy-d/e-cis-yohimbinoid07/24/2019

Contrary to usual observation, both venenatine (1a) and alstovenine (1b) give initially only a single oxindote derivative (3) instead of a pair. This oxindole displays unusual resistance to isomerisation in both acidic and basic media and is unique in its total insensitivity to pyridine. The unp...detailed

1055-75-0Relevant articles and documents

-

Chatterjee,A.,Roy,D.

, p. 1981 (1981)

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