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10315-89-6

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10315-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10315-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10315-89:
(7*1)+(6*0)+(5*3)+(4*1)+(3*5)+(2*8)+(1*9)=66
66 % 10 = 6
So 10315-89-6 is a valid CAS Registry Number.

10315-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylpropyl)piperidine

1.2 Other means of identification

Product number -
Other names N-isobutylpiperidine

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:10315-89-6 SDS

10315-89-6Downstream Products

10315-89-6Relevant articles and documents

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Marko,L.,Bakos,J.

, p. 411 - 414 (1974)

-

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King

, p. 898 (1951)

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A novel aminomethylation reaction of gaseous alkanes with tert-methylamine N-oxides via C-H bond activation by copper(II) salts

Taniguchi, Yuki,Horie, Shiro,Takaki, Ken,Fujiwara, Yuzo

, p. 137 - 142 (1995)

The Cu(OAc)2/CF3COOH (TFA) system catalyzes the aminomethylation of gaseous alkanes such as propane and ethane with trimethylamine N-oxide to give N,N-dimethylisobutylamine (1) and N,N-dimethylpropylamine (7), respectively.The corresponding trifluoroacetates are also formed as by-products from the reactions of methane and propane. Keywords: Copper acetate; Aminomethylation; Amine N-oxide; C-H bond activation; C-C bond formation; Alkane

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Stanley et al.

, p. 8,10 (1974)

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Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides

K?ring, Laura,Paradies, Jan,Sitte, Nikolai A.

supporting information, p. 1287 - 1300 (2022/01/20)

The development of the frustrated Lewis pair catalyzed hydrogenation of tertiary and secondary amides is reviewed. Detailed insight into our strategies in order to overcome challenges during the reaction development process is provided. Furthermore, the d

Catalytic hydrogenation of amides to amines under mild conditions

Stein, Mario,Breit, Bernhard

supporting information, p. 2231 - 2234 (2013/03/28)

Under (not so much) pressure: A general method for the hydrogenation of tertiary and secondary amides to amines with excellent selectivity using a bimetallic Pd-Re catalyst has been developed. The reaction proceeds under low pressure and comparatively low temperature. This method provides organic chemists with a simple and reliable tool for the synthesis of amines. Copyright

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