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1595-04-6

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1595-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1595-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1595-04:
(6*1)+(5*5)+(4*9)+(3*5)+(2*0)+(1*4)=86
86 % 10 = 6
So 1595-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H16/c1-3-4-7-11-8-5-6-10(2)9-11/h5-6,8-9H,3-4,7H2,1-2H3

1595-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name iso-Pentylbenzene

1.2 Other means of identification

Product number -
Other names Benzene, 1-butyl-3-methyl-

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:1595-04-6 SDS

1595-04-6Relevant articles and documents

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Merrill,R.E.,Negishi,E.

, p. 3452 - 3453 (1974)

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Alkylation-Terminated Catellani Reactions Using Alkyl Carbagermatranes

Jiang, Wei-Tao,Xiao, Bin,Xie, Xiu-Ying,Xu, Meng-Yu,Yang, Shuo

supporting information, p. 20450 - 20454 (2020/09/07)

The Catellani reaction has received substantial attention because it enables rapid multiple derivatization on aromatics. While using alkyl electrophiles to achieve ortho-alkylation was one of the earliest applications of the Catellani reaction, ipso-alkyl

meta-directing cobalt-catalyzed diels-alder reactions

Hilt, Gerhard,Janikowski, Judith,Hess, Wilfried

, p. 5204 - 5206 (2007/10/03)

(Chemical Equation Presented) Overcoming the ortho/para rule? The regioselectivity of Diels-Alder reactions with neutral electron demand between 1,3-dienes with alkynes can be controlled by simple cobalt diimine complexes so that the meta-substituted cycloadducts are generated in good yields and excellent regioselectivity (see scheme; DDQ=2,3-dichloro-5,6-dicyano-1,4- benzoquinone).

Reductive activation of arenes: XVII. Effect of methyl substituent in anion-radicals of tolunitriles on the mechanism of their reaction with alkyl bromides in liquid ammonia

Vaganova,Shteingarts

, p. 747 - 750 (2007/10/03)

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