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4184-34-3

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4184-34-3 Usage

General Description

"(24E)-3β-Hydroxy-9β,19-cyclo-5α-lanost-24-en-26-oic acid" is a specific type of biochemical compound that belongs to the category of lanostanes, which is a class of steroids whose structure is derived from lanosterol. Lanosterols are the primary building blocks for complex forms of steroids. This particular compound is characterized by its cyclo structure and hydroxy and oic acid functional groups. The hydroxy group enhances its polarity, which may influence its solubility in water, while the oic acid denotes the presence of a terminal carboxylic acid group. Typically, these compounds are found naturally in several varieties of plants and they usually exhibit varying degrees of biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 4184-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,8 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4184-34:
(6*4)+(5*1)+(4*8)+(3*4)+(2*3)+(1*4)=83
83 % 10 = 3
So 4184-34-3 is a valid CAS Registry Number.

4184-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (17β)-Estra-1,3,5(10)-triene-1,3,17-triol

1.2 Other means of identification

Product number -
Other names Magnesium diethanoate tetrahydrate

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:4184-34-3 SDS

4184-34-3Downstream Products

4184-34-3Relevant articles and documents

Reactions of Triterpenes: Part III - Partial Synthesis of 3β-Hydroxycycloart-24-en-26-al from Cycloart-24-ene-3β,26-diol

Anjaneyulu, V.,Prasad, K. Harischandra

, p. 1075 - 1076 (2007/10/02)

Oxidation of cycloart-24-ene-3β,26-diol (I) with DDQ or Ag2CO3/SiO2 in dry benzene gives only 3β-hydroxycycloart-24-en-26-al (II) whereas CrO3/pyridine oxidation of I yields II, mangiferonic acid (IV) and mangiferolic acid (V), besides a new ketoaldehyde (III).

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