96089-43-9

Basic information

• Product Name: Acetic acid, (4-formyl-3-hydroxyphenoxy)-, ethyl ester
• CAS NO: 96089-43-9
• Molecular Formula: C11H12O5
• Molecular Weight: 224.213
• Mol File: 96089-43-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Acetic acid, (4-formyl-3-hydroxyphenoxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, (4-formyl-3-hydroxyphenoxy)-, ethyl ester(96089-43-9)
• EPA Substance Registry System: Acetic acid, (4-formyl-3-hydroxyphenoxy)-, ethyl ester(96089-43-9)

Safety Data

• Hazardous Substances Data: 96089-43-9(Hazardous Substances Data)

Upstream product

• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 105-39-5 chloroacetic acid ethyl ester 
• 26562-26-5 3-bromo-2-ethoxy-propene 
• 105-36-2 ethyl bromoacetate 
• 623-48-3 ethyl iodoacetae 

Downstream Products

• 112683-76-8 1,3-dipropyl-6-amino-5-<<2-hydroxy-4-<(carboxymethyl)oxy>benzylidene>amino>uracil ethyl ester 
• 1353391-10-2 C₅₄H₉₀N₂O₈ 
• 83590-77-6 4-hydroxymethyl-3-methoxyphenoxyacetic acid 
• 58259-46-4 3-methoxy-4-formylphenoxyacetic acid ethyl ester 
• 119-41-5 7-ethoxycarbonylmethoxyflavone 
• 112683-67-7 1,3-dipropyl-8-{2-hydroxy-4-[(carbethoxymethyl)oxy]phenyl}xanthine 
• 112683-66-6 1,3-dipropyl-8-{2-hydroxy-4-[(carboxymethyl)oxy]phenyl}xanthine 
• 433212-88-5 (4-benzoxazol-2-yl-3-hydroxy-phenoxy)-acetic acid ethyl ester 
• 433212-92-1 (4-benzothiazol-2-yl-3-hydroxy-phenoxy)-acetic acid ethyl ester 

Relevant articles and documents

Aldehydes can switch the chemoselectivity of electrophiles in protein labeling

We show that the chemoselectivity of an electrophile in protein labeling can be promiscuous. An aldehyde enables switching of chemoselectivity of an epoxide and a sulfonate ester along with an enhanced rate of reaction. The chemical technology renders single-site installation of diverse probes on a protein and delivers analytically pure tagged proteins.

Preparation method of 4-hydroxymethyl-3-methoxyphenoxyacetic acid

The invention discloses a preparation method of 4-hydroxymethyl-3-methoxyphenoxyacetic acid, comprising the steps of a) subjecting the start material 2,4-dihydroxybenzaldehyde and halogenated ethyl acetate to nucleophilic substitution reaction under the a

Evidence of aggregation induced emission enhancement and keto-enol-tautomerism in a gallic acid derived salicylideneaniline gel

A novel salicylideneaniline type fluorescent organogelator based on a 3,4,5-(tri-dodecyloxy)benzoyl group immobilizes aromatic solvents. The resulting gels show enhancement in emission and thermochromic/non-photochromic behaviour during sol-to-gel transit