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4074-50-4

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4074-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4074-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4074-50:
(6*4)+(5*0)+(4*7)+(3*4)+(2*5)+(1*0)=74
74 % 10 = 4
So 4074-50-4 is a valid CAS Registry Number.

4074-50-4SDS

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-ethyl-3-hydroxyphenol

1.2 Other means of identification

Product number -
Other names 2-ethylbenzene-1,3-diol

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:4074-50-4 SDS

4074-50-4Relevant articles and documents

Vases and kites as cavitands

Moran, John R.,Ericson, John L.,Dalcanale, Enrico,Bryant, Judi A.,Knobler, Carolyn B.,Cram, Donald J.

, p. 5707 - 5714 (1991)

The syntheses, characterizations, and substituent effects on the vase vs kite conformations of 1-17 are described. These compounds are assembled by two-step syntheses from resorcinol (or 2-substituted derivatives) and aldehydes to form octols 18-26 in hig

Kolbe-Schmitt type reaction under ambient conditions mediated by an organic base

Sadamitsu, Yuta,Okumura, Akira,Saito, Kodai,Yamada, Tohru

supporting information, p. 9837 - 9840 (2019/08/20)

The combined use of an organic base for resorcinols realized a Kolbe-Schmitt type reaction under ambient conditions. When resorcinols (3-hydroxyphenol derivatives) were treated with DBU under a carbon dioxide atmosphere, nucleophilic addition to carbon dioxide proceeded to afford the corresponding salicylic acid derivatives in high yields.

QUINAZOLINE COMPOUNDS

-

Paragraph 00243; 00244, (2015/06/11)

The present invention relates to quinazoline compounds of formula I that function as inhibitors of RET (rearranged during transfection) kinase enzyme activity: (Formula (I)) wherein X, R1, R2, R3, R4, R5, R6 and R7 are each as defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, as well as other diseases or conditions in which RET kinase activity is implicated.

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