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103962-17-0

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103962-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103962-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,9,6 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103962-17:
(8*1)+(7*0)+(6*3)+(5*9)+(4*6)+(3*2)+(2*1)+(1*7)=110
110 % 10 = 0
So 103962-17-0 is a valid CAS Registry Number.

103962-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,2,3,3-tetrafluoropropoxy)-benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(2,2,3,3-Tetrafluoro-propoxy)-benzaldehyde

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:103962-17-0 SDS

103962-17-0Relevant articles and documents

Alpha-aminoamide derivative and application thereof

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Paragraph 0264; 0266; 0267, (2019/02/04)

The invention discloses an alpha-aminoamide derivative and application thereof. Specifically, the invention relates to a novel alpha-aminoamide derivative and a pharmaceutical composition containing the compound. The invention also relates to a method for

Piperidinyl-and piperazinyl-sulfonylmethyl hydroxamic acids and their use as protease inhibitors

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Page 305; 349, (2010/02/10)

This invention is directed generally to proteinase (also known as “protease”) inhibitors, and, more particularly, to piperidinyl- and piperazinyl-sulfonylmethyl hydroxamic acids that, inter alia, inhibit matrix metalloproteinase (also known as “matrix metalloprotease” or “MMP”) activity and/or aggrecanase activity. Such hydroxamic acids generally correspond in structure to the following formula: (wherein A1, A2, Y, E1, E2, E3, and Rx are as defined in this specification), and further include salts of such compounds. This invention also is directed to compositions of such hydroxamic acids, intermediates for the syntheses of such hydroxamic acids, methods for making such hydroxamic acids, and methods for treating conditions (particularly pathological conditions) associated with MMP activity and/or aggrecanase activity.

Triazole antifungal agent

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, (2008/06/13)

A triazole compound having the formula: STR1 wherein Ar1 represents an optionally substituted phenyl, Ar2 represents an optionally substituted phenyl, R0 represents a hydrogen atom or a lower alkyl; R1 represents a lower alkyl; R2 to R5 represent a hydrogen atom or an unsubstituted or halo substituted alkyl, n represents 0 to 2; p represents 0 or 1; q, r and s each represent 0 to 2; and A represents a 1,3-dioxan-5-yl. The triazole compound of the present invention exhibits an excellent antifungal activity.

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