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77740-81-9

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77740-81-9 Usage

General Description

2-Methyl-1-(naphthalen-2-yl)-2-nitropropan-1-ol is a chemical compound with a molecular formula C13H15NO3. It consists of a naphthalene group attached to a nitropropanol moiety. 2-Methyl-1-(naphthalen-2-yl)-2-nitropropan-1-ol is a nitro alcohol, with a nitro group and an alcohol functional group in its structure. It is commonly used as a building block in organic synthesis, and its derivatives have been studied for various pharmaceutical and industrial applications. The compound exhibits some biological activity and is a potential candidate for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 77740-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,4 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77740-81:
(7*7)+(6*7)+(5*7)+(4*4)+(3*0)+(2*8)+(1*1)=159
159 % 10 = 9
So 77740-81-9 is a valid CAS Registry Number.

77740-81-9SDS

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-methyl-1-naphthalen-2-yl-2-nitropropan-1-ol

1.2 Other means of identification

Product number -
Other names 2-Naphthalenemethanol,a-(1-methyl-1-nitroethyl)

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:77740-81-9 SDS

77740-81-9Downstream Products

77740-81-9Relevant articles and documents

Calcium receptor antagonist

-

Page 20, (2010/11/30)

A compound of the formula [I] wherein R1 is optionally substituted aryl group or optionally substituted heteroaryl group; R2 is optionally substituted C1-6 alkyl group, C3-7 cycloalkyl group and the like; R3 is hydrogen atom, C1-6 alkyl group, hydroxyl group and the like; R4 is hydrogen atom, C1-6 alkyl group and the like; R5 and R6 are each C1-6 alkyl group and the like; R7 is optionally substituted aryl group or optionally substituted heteroaryl group; X1, X2 and X3 are each C1-6 alkylene group and the like; and X4 and X5 are each a single bond, methylene group and the like, a salt thereof, a solvate thereof or a prodrug thereof, and a pharmaceutical composition containing the compound, particularly a calcium receptor antagonist and a therapeutic agent for osteoporosis, are provided. The compound of the present invention is useful as a therapeutic drug of diseases accompanied by abnormal calcium homeostasis, or osteoporosis, hypoparathyreosis, osteosarcoma, periodontal disease, bone fracture, steoarthrosis, chronic rheumatoid arthritis, Paget's disease, humoral hypercalcemia, autosomal dominant hypocalcemia and the like. In addition, an intermediate for the compound is provided.

Preparation of 4-Aryl-1,2,3,4-tetrahydro-3,3-dimethylisoquinolines and 1,2,3,4-Tetrahydro-3,3-dimethyl-4-phenylbenzisoquinolines

Bobowski, George,Gottlieb, Jeffrey M.,West, Barbara

, p. 1563 - 1568 (2007/10/02)

Synthetic procedures to prepare a number of 4-aryl-1,2,3,4-tetrahydro-3,3-dimethylisoquinolines and their benzo-homologues 3 through a series of intermediates are described.The condensation of α-(1-amino-1-methylethyl)arylmethanols 5 with arylaldehydes 6

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