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3007-70-3

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3007-70-3 Usage

General Description

N-heptylaniline is a chemical compound composed of a heptyl group and an aniline group. It is a clear to pale yellow liquid with a molecular formula of C13H19N and a molecular weight of 193.29 g/mol. N-heptylaniline is commonly used in the manufacturing of dyes, pigments, and pharmaceuticals. It is also utilized in the production of rubber and plastic chemicals, as well as in the synthesis of other organic compounds. N-heptylaniline is considered to be a hazardous substance and should be handled with care, as it can cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 3007-70-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3007-70:
(6*3)+(5*0)+(4*0)+(3*7)+(2*7)+(1*0)=53
53 % 10 = 3
So 3007-70-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H21N/c1-2-3-4-5-9-12-14-13-10-7-6-8-11-13/h6-8,10-11,14H,2-5,9,12H2,1H3

3007-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-heptylaniline

1.2 Other means of identification

Product number -
Other names Heptylamine,N-phenyl

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:3007-70-3 SDS

3007-70-3Relevant articles and documents

Reusable Co-nanoparticles for general and selectiveN-alkylation of amines and ammonia with alcohols

Beller, Matthias,Gawande, Manoj B.,Jagadeesh, Rajenahally V.,Kadam, Ravishankar G.,Li, Xinmin,Ma, Zhuang,Petr, Martin,Zbo?il, Radek,Zhou, Bei

, p. 111 - 117 (2022/01/06)

A general cobalt-catalyzedN-alkylation of amines with alcohols by borrowing hydrogen methodology to prepare different kinds of amines is reported. The optimal catalyst for this transformation is prepared by pyrolysis of a specific templated material, which is generatedin situby mixing cobalt salts, nitrogen ligands and colloidal silica, and subsequent removal of silica. Applying this novel Co-nanoparticle-based material, >100 primary, secondary, and tertiary amines includingN-methylamines and selected drug molecules were conveniently prepared starting from inexpensive and easily accessible alcohols and amines or ammonia.

Iron-catalyzed N-alkylation of aromatic amines via borrowing hydrogen strategy

Chen, Hui,Wang, Qingfu,Liu, Tingting,Chen, Haitao,Zhou, Duo,Qu, Fengbo

, p. 877 - 884 (2021/02/16)

Earth-abundant transition metals could be used as a noble metal replacement in catalysis not only for different catalytic reactivity but environmentally benign methodology. We report here on the iron-catalyzed synthesis of N-alkylated amines via borrowing hydrogen strategy and differently functionalized aniline derivatives are alkylated in good yields.

Cobalt encapsulated in N?doped graphene sheet for one-pot reductive amination to synthesize secondary amines

Liu, Lin,Li, Wenxiu,Qi, Ran,Zhu, Qingqing,Li, Jing,Fang, Yuzhen,Kong, Xiangjin

, (2021/03/14)

To develop an efficient base-metal reductive amination catalyst for synthesis of secondary amines is still a major challenge. In this study, an efficient N-doped graphene sheet-coated cobalt catalyst (Co@CN-800) was developed through a simple pyrolysis process, which could gave 99.5 % yield of N-benzylaniline by one-pot reductive amination of nitrobenzene with benzaldehyde during at least 5 cycles. Catalyst characterization and control experiments confirmed that the robust catalytic performance of the catalyst is probably due to the synergy effect of in situ generated Co-Nx encapsulated in N?doped graphene layer and appropriate meso-pore structure. Additionally, The substrate adaptability of the catalyst was proved since a variety of corresponding secondary amines were smoothly obtained under relatively mild conditions, which makes the secondary amine synthesis strategy based on Co@CN-800 shows excellent application prospect.

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