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4-AMINO-6-TERT-BUTYLPYRIMIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3435-27-6

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3435-27-6 Usage

Uses

4-Amino-6-(tert-butyl)pyrimidine is a useful research intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 3435-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3435-27:
(6*3)+(5*4)+(4*3)+(3*5)+(2*2)+(1*7)=76
76 % 10 = 6
So 3435-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H13N3/c1-8(2,3)6-4-7(9)11-5-10-6/h4-5H,1-3H3,(H2,9,10,11)

3435-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-tert-butylpyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 6-tert-butyl-pyrimidin-4-ylamine

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:3435-27-6 SDS

3435-27-6Downstream Products

3435-27-6Relevant academic research and scientific papers

HERBICIDAL COMPOUNDS

-

Page/Page column 43, (2015/03/13)

The invention relates to pyrrolone compounds of the formula (I) wherein X, R1, R2, R3, Ra, Rc and Rd are as defined in the specification. Furthermore, the present invention relates to processes and intermediates for making compounds of formula (I), to herbicidal compositions comprising these compounds and to methods of using these compounds to control plant growth.

The Chichibabin amination of 4-phenyl- and 4-tert-butyl-pyrimidine

Breuker, J.,Plas, H. C. van der

, p. 367 - 372 (2007/10/02)

During a study on the amination of 4-phenylpyrimidine in potassium amide/liquid ammonia it was found that the extent to which the SN(ANRORC) mechanism operates in the amination largely depends upon whether an ammonium salt is used in quenching the reaction.The composition of the ?-adduct mixture, the structure of the open-chain intermediates, the inhibition of the SN(ANRORC) mechanism and the course of the amination in apolar solvents have been investigated.In addition, it has been found that, in the amination of 4-tert-butylpyrimidine, the SN(ANRORC) mechanism occurs to only a very limited extent.

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