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6135-22-4

6135-22-4

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6135-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6135-22-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6135-22:
(6*6)+(5*1)+(4*3)+(3*5)+(2*2)+(1*2)=74
74 % 10 = 4
So 6135-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO/c1-9(2)7-4-3-5-8(10)6-7/h6H,3-5H2,1-2H3

6135-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dimethylamino)cyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names EINECS 228-106-4

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:6135-22-4 SDS

6135-22-4Relevant articles and documents

Formation of benzocyclobutenes from substituted oxocycloocta-2,8-diene-1,2-dicarboxylates Dedicated to the memory of Professor Alan Roy Katritzky

Bezen?ek, Jure,Gro?elj, Uro?,Po?kaj, Marta,Svete, Jurij,Stanovnik, Branko

, p. 5705 - 5708 (2015/09/29)

Substituted benzocyclobutenes were isolated from the reaction of substituted oxocycloocta-2,8-diene-1,2-dicarboxylates with DMAD which were themselves formed by the microwave assisted [2+2] cycloaddition of cyclic enaminones to dimethyl acetylenedicarboxylate. The high pressure hydrogenation of (1E,2Z)-dimethyl 3-(dimethylamino)-7-oxocycloocta-2,8-diene-1,2-dicarboxylate gave oxabicyclo[3.3.1]non-3-ene-2,3-dicarboxylates, while use of low pressure hydrogenation resulted in only the carbonyl group being reduced to give the corresponding hydroxyl derivative which was proposed as an intermediate of the oxabicyclo[3.3.1]nonanes formed using high pressure hydrogenation.

Enone Mesylates. Precursors to β-Substituted Cyclohexenones

Kowalski, Conrad J.,Fields, Kevin W.

, p. 197 - 201 (2007/10/02)

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