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16545-68-9

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16545-68-9 Usage

Uses

Cyclopropanol is a basic building block.

Check Digit Verification of cas no

The CAS Registry Mumber 16545-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,4 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16545-68:
(7*1)+(6*6)+(5*5)+(4*4)+(3*5)+(2*6)+(1*8)=119
119 % 10 = 9
So 16545-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O/c4-3-1-2-3/h3-4H,1-2H2

16545-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopropanol

1.2 Other means of identification

Product number -
Other names Hydroxy-cyclopropan

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:16545-68-9 SDS

16545-68-9Relevant articles and documents

-

DePuy,C.H. et al.

, p. 3616 - 3617 (1961)

-

ENZYMATIC HYDROLYSIS OF CYCLOPROPYL ACETATE, A FACILE METHOD FOR MEDIUM- AND LARGE-SCALE PREPARATIONS OF CYCLOPROPANOL

Jongejan, Jaap A.,Duine, Johannis A.

, p. 2767 - 2768 (1987)

Enzymatic hydrolysis of cyclopropyl acetate at neutral pH, using commercially available enzyme preparations, results in a mixture from which cyclopropanol can be isolated by simple extraction.

SELECTIVE POTASSIUM CHANNEL AGONISTS

-

Page/Page column 32-33, (2019/11/12)

Selective potassium channel agonists and methods of use thereof are disclosed. A compound, or a pharmaceutically acceptable salt thereof, having a formula (I) wherein R1 is H or optionally-substituted alkyl; R2 is optionally-substituted C1-C6 alkyl or optionally- substituted cyclopropyl; R3 and R4 are each independently H or optionally- substituted alkyl; R5 is H, optionally-substituted alkyl, acyl, or alkoxycarbonyl; R6 and R7 are each independently H, optionally- substituted alkyl, or R6 and R7 together form a carbocycle; R8 is substituted phenyl or optionally-substituted pyridinyl, provided that if R8 is substituted phenyl, then R2 is optionally-substituted cyclopropyl; and R9, R10 and R11 are each independently H, halo, or optionally- substituted alkyl.

ALK KINASE INHIBITOR, AND PREPARATION METHOD AND USE THEREOF

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Paragraph 0103; 0104; 0105, (2017/04/18)

An ALK kinase inhibitor compound as represented by Formula I, pharmaceutical composition containing the compound, and preparation method and use thereof in the preparation of drugs serving as an ALK inhibitor for treating cancer.

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