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2878-14-0

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2878-14-0 Usage

Description

2-Methylallylamine, also known as 2-Methyl-2-propen-1-amine, is an organic compound with the chemical formula C4H9N. It is a clear colorless liquid and serves as an important intermediate in the synthesis of various pharmaceutical compounds.

Uses

Used in Pharmaceutical Industry:
2-Methylallylamine is used as an intermediate for the synthesis of urea-containing FK506 binding protein inhibitors. These inhibitors play a crucial role in modulating the immune system and have applications in treating autoimmune diseases and preventing organ transplant rejection.
Additionally, 2-Methylallylamine is used to prepare benzothiazepine dioxides, which exhibit HIV-1 protease inhibitory activities. These compounds are essential in the development of antiretroviral drugs for the treatment of HIV/AIDS.

Check Digit Verification of cas no

The CAS Registry Mumber 2878-14-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2878-14:
(6*2)+(5*8)+(4*7)+(3*8)+(2*1)+(1*4)=110
110 % 10 = 0
So 2878-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H9N/c1-4(2)3-5/h1,3,5H2,2H3/p+1

2878-14-0 Well-known Company Product Price

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  • TCI America

  • (M2726)  2-Methylallylamine  >98.0%(GC)(T)

  • 2878-14-0

  • 1mL

  • 590.00CNY

  • Detail
  • TCI America

  • (M2726)  2-Methylallylamine  >98.0%(GC)(T)

  • 2878-14-0

  • 5mL

  • 1,990.00CNY

  • Detail

2878-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylprop-2-en-1-amine

1.2 Other means of identification

Product number -
Other names 2-Methylallylamine

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:2878-14-0 SDS

2878-14-0Relevant articles and documents

-

Nishikawa,Y. et al.

, p. 155 - 160 (1972)

-

Direct catalytic synthesis of unprotected 2-amino-1-phenylethanols from alkenes by using iron(II) phthalocyanine

Legnani, Luca,Morandi, Bill

supporting information, p. 2248 - 2251 (2016/02/18)

Aryl-substituted amino alcohols are privileged scaffolds in medicinal chemistry and natural products. Herein, we report that an exceptionally simple and inexpensive FeII complex efficiently catalyzes the direct transformation of simple alkenes into unprotected amino alcohols in good yield and perfect regioselectivity. This new catalytic method was applied in the expedient synthesis of bioactive molecules and could be extended to aminoetherification.

SUBSTITUTED QUINAZOLINE DERIVATIVES AND THEIR USE AS INHIBITORS

-

, (2008/06/13)

The use of a compound of formula (I) 1 or a salt, ester or amide thereof; where X is O, or S, S(O) or S(O)2, or NR6 where R6 is hydrogen or C1-6 alkyl,; R5 is an optionally substituted 5-membered heteroaromatic ring, R1, R2 ,R3, R4 are independently selected from various specified moieties, in the preparation of a medicament for use in the inhibition of aurora 2 kinase. Certain compounds are novel and these, together with pharmaceutical compositions containing them are also described and claimed

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