Cas 438532-37-7,3-(2,4-DIFLUORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE

438532-37-7

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Basic information

Product Name: 3-(2,4-DIFLUORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE
Synonyms: 3-(2,4-DIFLUORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE;AKOS B000990;ART-CHEM-BB B000990;ALD-N000505;ARONIS015561;MLS000324558;Oprea1_386152;SMR000159832
CAS NO:438532-37-7
Molecular Formula: C15H12F2O3
Molecular Weight: 278.25
EINECS: N/A
Product Categories: N/A
Mol File: 438532-37-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-(2,4-DIFLUORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE(CAS DataBase Reference)
NIST Chemistry Reference: 3-(2,4-DIFLUORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE(438532-37-7)
EPA Substance Registry System: 3-(2,4-DIFLUORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE(438532-37-7)

Safety Data

Hazard Codes: Xi
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: IRRITANT
PackingGroup: N/A
Hazardous Substances Data: 438532-37-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 438532-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,5,3 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 438532-37:
(8*4)+(7*3)+(6*8)+(5*5)+(4*3)+(3*2)+(2*3)+(1*7)=157
157 % 10 = 7
So 438532-37-7 is a valid CAS Registry Number.

438532-37-7Upstream product

438532-37-7Downstream Products

438532-37-7Relevant academic research and scientific papers

Alkylation of NH-, OH-, and SH-acids in the presence of potassium carbonate: 1. Functionalization of chloromethyl group of alkoxy-substituted aromatic aldehydes

Khachatryan,Razinov,Kolotaev,Belus?,Matevosyan

, p. 395 - 404 (2015/10/29)

An easily scalable, economocal, and more safe method for the preparation of 3-chloromethyl-4-methoxybenzaldehyde was developed. The latter was subjected to reactions with NH-, OH-, and SH-acids in the presence of potassium carbonate to obtain new aromatic aldehydes in high yields.

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