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474-08-8

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474-08-8 Usage

General Description

Demissidine is a chemical compound that belongs to the class of organic compounds known as benzimidazoles. This chemical group is characterized by a benzene ring fused to an imidazole ring. It has been commonly used in laboratories and exhibits fungicidal properties, often utilized in the control of many fungal diseases. In terms of its structure, demissidine is a monocyclic compound that contains a benzimidazole skeleton with an amino functional group. It is important to handle this chemical with care as its effects on human health or the environment have not been fully studied.

Check Digit Verification of cas no

The CAS Registry Mumber 474-08-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 474-08:
(5*4)+(4*7)+(3*4)+(2*0)+(1*8)=68
68 % 10 = 8
So 474-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C27H45NO/c1-16-5-8-23-17(2)25-24(28(23)15-16)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h16-25,29H,5-15H2,1-4H3

474-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name DEMISSIDINE

1.2 Other means of identification

Product number -
Other names SOLANIN D

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:474-08-8 SDS

474-08-8Downstream Products

474-08-8Relevant articles and documents

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Burn,Rigby

, p. 963 (1953)

-

-

Weisenborn,Burn

, p. 259,262 (1953)

-

Confirmation of Structure of Isosolacapine: Stereochemistry at Ring Juncture of Indolizidine Moiety of 22βH Solanidanes by 13C and 1H NMR Spectroscopy

Chakravarty, Ajit K.,Pakrashi, Satyesh C.

, p. 311 - 313 (2007/10/02)

Isosolacapine, a minor steroidal alkaloid of Solanum pseudocapsicum, earlier assigned structure 3, possesses a novel 22β N stereochemistry in a 22,26-epiminocholestane skeleton.This alkaloid has now been isolated from Solanum capsicastrum and its structure confirmed by its conversion to solanogantamine (8), a 22αH solanidane derivative ex Solanum giganteum.The ring-juncture stereochemistry of the indolizidine moiety of 22β H solanidanes, in general, has been elucidated on 13C and 1H NMR spectral evidences.

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