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1482-78-6

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1482-78-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1482-78-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1482-78:
(6*1)+(5*4)+(4*8)+(3*2)+(2*7)+(1*8)=86
86 % 10 = 6
So 1482-78-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H32O3/c1-13(22)24-15-8-10-20(2)14(12-15)4-5-16-17-6-7-19(23)21(17,3)11-9-18(16)20/h14-18H,4-12H2,1-3H3/t14-,15-,16+,17+,18+,20+,21+/m1/s1

1482-78-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-acetoxy-(5α)-androstan-17-one

1.2 Other means of identification

Product number -
Other names 5BETA-ANDROSTAN-3ALPHA-OL-17-ONE 3-ACETATE

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:1482-78-6 SDS

1482-78-6Relevant articles and documents

A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of α,β-unsaturated ketoximes

Yan, Zhaohua,Xu, Yun,Tian, Weisheng

supporting information, p. 7186 - 7189 (2015/02/02)

The reaction of α,β-unsaturated ketoximes with fluoroalkanosulfonyl fluorides in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) underwent the Beckmann rearrangement smoothly to afford the corresponding acid-sensitive enamides in moderate to excellent yields, which provides a new efficient method for the preparation of acid-sensitive enamides.

Process for the preparation of 17β-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone

-

, (2008/06/13)

A new process utilizing certain novel intermediates for the preparation of 17β-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone is described herein. The procedure utilizes readily available and inexpensive sarsasaponin as starting material.

4-CHLOROSTEROIDS. SYNTHESIS OF 4-BETA-CHLORO-DEHYDROISOANDROSTERONE ACETATE AND OF 4-CHLORO-4-ANDROSTEN-3 BETA-OL-17-ONE ACETATE.

CAMERINO,DECASTIGLIONE,BOSISIO

, p. 312 - 323 (2007/10/06)

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