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144314-35-2

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144314-35-2 Usage

Description

1-Naphthalenecarboxamide, 1,2-dihydro-N-(phenylmethyl)is a chemical compound with the molecular formula C17H17NO. It is a white to off-white crystalline powder that is commonly used as an intermediate in the production of various organic compounds. 1-Naphthalenecarboxamide, 1,2-dihydro-N-(phenylmethyl)is also known for its potential pharmaceutical properties and is commonly used in the synthesis of pharmaceutical drugs. Additionally, it is used in the production of agrochemicals and other specialty chemicals. 1-Naphthalenecarboxamide, 1,2-dihydro-N-(phenylmethyl)is considered to be non-toxic and non-irritating, making it a relatively safe compound to handle when following proper safety guidelines.

Uses

Used in Pharmaceutical Industry:
1-Naphthalenecarboxamide, 1,2-dihydro-N-(phenylmethyl)is used as an intermediate in the synthesis of pharmaceutical drugs for its potential pharmaceutical properties.
Used in Agrochemical Industry:
1-Naphthalenecarboxamide, 1,2-dihydro-N-(phenylmethyl)is used in the production of agrochemicals, contributing to the development of various agricultural products.
Used in Specialty Chemicals Industry:
1-Naphthalenecarboxamide, 1,2-dihydro-N-(phenylmethyl)is used in the production of specialty chemicals, serving as an important component in the synthesis of specific chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 144314-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,3,1 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144314-35:
(8*1)+(7*4)+(6*4)+(5*3)+(4*1)+(3*4)+(2*3)+(1*5)=102
102 % 10 = 2
So 144314-35-2 is a valid CAS Registry Number.

144314-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-1,2-dihydronaphthalene-1-carboxamide

1.2 Other means of identification

Product number -
Other names -

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:144314-35-2 SDS

144314-35-2Downstream Products

144314-35-2Relevant articles and documents

Benzylic functionalization of (η6-alkylarene)chromium tricarbonyl complexes

Kalinin, Valery N.,Cherepanov, Il'ya A.,Moiseev, Sergey K.

, p. 437 - 455 (1997)

A general method for the regioselective benzylic metallation of (η6-alkylarene)chromium tricarbonyl complexes on the action of lithium amides in THF under very mild conditions has been developed. Transmetallation reactions of the lithium derivatives thus obtained produce the corresponding benzylic organotin, zinc and copper chromium tricarbonyl complexes. Methods for the preparative benzylic functionalization of (η6-alkylarene)chromium tricarbonyl complexes have been developed, including carboxylation, α-hydroxyalkylation, γ-carbonylation, acylation, arylation, vinylation, heteroarylation and alkylation procedures. 5-Acetoxy-3-benzyl-1,4-methano-2,3,4,5-tetrahydro-1H-3-benzazepine has been prepared using the benzylic lithium derivative of the (η6-alkylarene)chromium tricarbonyl complex at the key step. This compound is a representative of the major class of physiologically active compounds known as C-norbenzomorphans.

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