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2-nitrocyclohex-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51254-77-4

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51254-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51254-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,5 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51254-77:
(7*5)+(6*1)+(5*2)+(4*5)+(3*4)+(2*7)+(1*7)=104
104 % 10 = 4
So 51254-77-4 is a valid CAS Registry Number.

51254-77-4SDS

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 2-nitrocyclohex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 2-nitro-2-cyclohexene-1-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:51254-77-4 SDS

51254-77-4Relevant academic research and scientific papers

TRIFLUOROACETOXY-PHENYLSELENATION OF NITROOLEFINS REGIOSELECTIVE PREPARATION OF NITROALLYLIC ALCOHOL DERIVATIVES AND THEIR USE AS MULTIPLE COUPLING REAGENTS

Seebach, Dieter,Calderari, Giorgio,Knochel, Paul

, p. 4861 - 4872 (2007/10/02)

It has been shown in previous papers that the pivalate of 2-nitro-2-propen-1-ol (NPP, 1), a nitroolefin with allylic leaving group, can be used as a versatile multiple coupling reagent.The present contribution describes the preparation of analogues, subst

SYNTHESIS AND REACTIONS OF SUBSTITUTED NITRO-ALLYLATING REAGENTS

Knochel, Paul,Seebach, Dieter

, p. 3897 - 3900 (2007/10/02)

Nitro-cyclohexenylation and α-phenyl-nitro-allylation of nucleophilic centres are achieved (see 11-16) whith the nitroallyl pivalates 2 and 5, and with the chloride 3, which are in turn prepared from the diols 9 and 10, respectively.

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