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3186-86-5

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3186-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3186-86-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3186-86:
(6*3)+(5*1)+(4*8)+(3*6)+(2*8)+(1*6)=95
95 % 10 = 5
So 3186-86-5 is a valid CAS Registry Number.

3186-86-5SDS

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 3β-hydroxylupane

1.2 Other means of identification

Product number -
Other names lupanol-(3β)

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:3186-86-5 SDS

3186-86-5Relevant articles and documents

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Kulshreshtha,D.K.

, p. 1783 - 1785 (1977)

-

-

Faparusi,S.I.,Bassir,O.

, p. 3083 - 3084 (1972)

-

Preparation and molecular rearrangement of 2α, 3α-epoxy lupan-1-one catalysed by boron trifluoride and by ultraviolet irradiation+

Bose,Chanda

, p. 510 - 514 (2007/10/03)

Using lupeol 7 as lead compound 2α, 3α-epoxy lupan-1-one 11 has been synthesised by a sequence of reactions. Boron trifluoride catalysed molecular rearrangement of 11 in benzene yields 2-formyl-A-nor-lupan-1-one 15 (enolized). Same rearrangement is also achieved in dioxane under photolytic condition.

The synthesis of nor- and bisnorlupanes

Wahhab, Amal,Ottosen, Margaret,Bachelor, Frank W.

, p. 570 - 577 (2007/10/02)

In course of our studies on geochemical biomarkers we required a series of lupane standards.We report here an efficient synthesis of lupane (1) in three steps from betulin (3) in an overall yield of 47.2 percent. 17β(H)-28-Norlupane (2) was obtained in 90

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