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6284-27-1

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6284-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6284-27-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6284-27:
(6*6)+(5*2)+(4*8)+(3*4)+(2*2)+(1*7)=101
101 % 10 = 1
So 6284-27-1 is a valid CAS Registry Number.

6284-27-1SDS

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 2-(3-bromo-2-hydroxypropyl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-(3-bromo-2-hydroxypropyl)-1h-isoindole-1,3(2h)-dione

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:6284-27-1 SDS

6284-27-1Downstream Products

6284-27-1Relevant articles and documents

Taking advantage of lithium monohalocarbenoid intrinsic α-elimination in 2-MeTHF: controlled epoxide ring-openingen routeto halohydrins

Ielo, Laura,Miele, Margherita,Pillari, Veronica,Senatore, Raffaele,Mirabile, Salvatore,Gitto, Rosaria,Holzer, Wolfgang,Alcántara, Andrés R.,Pace, Vittorio

supporting information, p. 2038 - 2043 (2021/03/16)

The intrinsic degradative α-elimination of Li carbenoids somehow complicates their use in synthesis as C1-synthons. Nevertheless, we herein report how boosting such an α-elimination is a straightforward strategy for accomplishing controlled ring-opening of epoxides to furnish the corresponding β-halohydrins. Crucial for the development of the method is the use of the eco-friendly solvent 2-MeTHF, which forces the degradation of the incipient monohalolithium, due to the very limited stabilizing effect of this solvent on the chemical integrity of the carbenoid. With this approach, high yields of the targeted compounds are consistently obtained under very high regiocontrol and, despite the basic nature of the reagents, no racemization of enantiopure materials is observed.

A straightforward and general access to α-phthalimido-α′- substituted propan-2-ones

Pace, Vittorio,Holzer, Wolfgang

supporting information; experimental part, p. 5106 - 5109 (2012/10/08)

The regioselective ring opening of the commercially available N-(2,3-epoxypropyl)phthalimide with different nucleophiles, to obtain the corresponding phthalimidopropan-2-ols (including a challenging fluorohydrin) followed by the Dess-Martin periodinane ox

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