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82354-38-9

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82354-38-9 Usage

General Description

Humantenmine is a synthetic chemical compound used in the pharmaceutical industry as an antifungal agent. It is classified as an azole antifungal medication, working by inhibiting the synthesis of ergosterol, a key component of the fungal cell membrane. This action disrupts the structure and function of the fungal cells, ultimately leading to their death. Humantenmine is commonly used to treat various fungal infections, such as athlete's foot, ringworm, and vaginal yeast infections. It is available in various forms, including creams, ointments, and oral tablets, and is generally well-tolerated with few side effects. However, it may interact with certain medications and should be used with caution in individuals with certain medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 82354-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,5 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82354-38:
(7*8)+(6*2)+(5*3)+(4*5)+(3*4)+(2*3)+(1*8)=129
129 % 10 = 9
So 82354-38-9 is a valid CAS Registry Number.

82354-38-9SDS

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 Humantenmine

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:82354-38-9 SDS

82354-38-9Downstream Products

82354-38-9Relevant articles and documents

Divergent Entry to Gelsedine-Type Alkaloids: Total Syntheses of (-)-Gelsedilam, (-)-Gelsenicine, (-)-Gelsedine, and (-)-Gelsemoxonine

Wang, Pingluan,Gao, Yang,Ma, Dawei

supporting information, p. 11608 - 11612 (2018/09/21)

The gelsedine-type alkaloids possess a common oxabicyclo[3.2.2]nonane core and spiro-N-methoxyindolinone moiety along with a diversely functionalized heterocycle embedded in the compact framework. Herein we disclose a divergent entry to gelsedine-type alk

Spectroscopic analyses and chemical transformation for structure elucidation of two novel indole alkaloids from Gelsemium elegans

Yamada, Yousuke,Kitajima, Mariko,Kogure, Noriyuki,Wongseripipatana, Sumphan,Takayama, Hiromitsu

body text, p. 3341 - 3344 (2009/09/05)

Two new monoterpenoid oxindole alkaloids, gelsevanillidine (1) having an additional vanillin residue on gelsenicine-type alkaloid and gelseoxazolidinine (2) possessing an unusual oxazolidine ring, were isolated from Gelsemium elegans. To confirm their str

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