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1427-61-8

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1427-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427-61-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1427-61:
(6*1)+(5*4)+(4*2)+(3*7)+(2*6)+(1*1)=68
68 % 10 = 8
So 1427-61-8 is a valid CAS Registry Number.

1427-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 10β-fluoroestra-1,4-diene-17β-ol-3-one

1.2 Other means of identification

Product number -
Other names 10β-Fluoro-3-oxo-1,4-estradien-17β-ol

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:1427-61-8 SDS

1427-61-8Upstream product

1427-61-8Downstream Products

1427-61-8Relevant articles and documents

Fluorination of steroid estrogens with Selectfluor??: Elucidation of regio- and stereoselectivity

Bogautdinov, Roman P.,Fidarov, Alan F.,Morozkina, Svetlana N.,Zolotarev, Andrei A.,Starova, Galina L.,Selivanov, Stanislav I.,Shavva, Alexander G.

, p. 218 - 222 (2014)

Two steroid estrogens, natural estradiol and 8?±-estradiol, were fluorinated using Selectfluor?? in ionic liquid. Unexpectedly, mostly products of fluorination at position C-10 were isolated instead of corresponding fluorophenols, as it was reported previ

Efficient synthesis of 4-fluorocyclohexa-2,5-dienone derivatives using n-fluoro-1,4-diazoniabicyclo[2.2.2]octane salt analogues

Stavber, Stojan,Jereb, Marjan,Zupan, Marko

, p. 1375 - 1378 (2007/10/03)

4-Fluorocyclohexa-2,5-dienone derivatives were obtained in high yield by reaction of para substituted phenols with 1-fluoro-4-chloromethyl-1,4- diazoniabicyclo[2.2.2]octane bis(tetra-fluoro-borate) (1a, Selectfluor(TM) F- TEDA-BF4) or its 4-hyd

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