103024-85-7

Basic information

• Product Name: BENZYLOXY-3-CHLORO-2-PROPANOL
• Synonyms: BENZYLOXY-3-CHLORO-2-PROPANOL
• CAS NO: 103024-85-7
• Molecular Weight: 0
• Mol File: 103024-85-7.mol
• Article Data: 35

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZYLOXY-3-CHLORO-2-PROPANOL(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYLOXY-3-CHLORO-2-PROPANOL(103024-85-7)
• EPA Substance Registry System: BENZYLOXY-3-CHLORO-2-PROPANOL(103024-85-7)

Safety Data

• Hazardous Substances Data: 103024-85-7(Hazardous Substances Data)

Upstream product

• 106-89-8 epichlorohydrin 
• 100-51-6 benzyl alcohol 
• 2930-05-4 Benzyloxymethyl-oxiran 
• 18001-18-8 allyldimethylphenylsilane 
• 17922-43-9 allyldiphenyl(methyl)silane 
• 24400-84-8 allyl triisopropylsilane 
• 762-72-1 allyl-trimethyl-silane 
• 13071-59-5 3-benzyloxypropan-1,2-diol 
• 100-39-0 benzyl bromide 
• 67843-74-7 (S)-epichlorohydrin 
• 13991-52-1 1-chloro-2-hydroxy-3-phenylmethoxypropane 
• 51594-55-9 (R)-(-)-epichlorohydrin 
• 3536-96-7 vinylmagnesium chloride 
• 2930-05-4 (S)-benzyl glycidyl ether 

Downstream Products

• 50610-95-2 1-benzyloxy-2-hydroxy-3-phenoxypropane 
• 64341-54-4 4-(1-benzyloxy-3-chloroisopropoxy)azetidin-2-one 
• 93728-27-9 1-benzyloxy-3-(2-methoxy-phenoxy)-propan-2-ol 
• 2930-05-4 (S)-benzyl glycidyl ether 
• 75507-17-4 benzyl 2,4,7,10,13-pentaoxacyclopentadecan-2-ylmethyl ether 
• 1441160-78-6 tert-butyl 4-[acetyl(tert-butoxycarbonyl)amino]-6-(benzyloxymethyl)-3-oxo-5H-1,2,4-triazine-2-carboxylate 
• 1441160-75-3 N-[6-(benzyloxymethyl)-3-oxo-2,5-dihydro-1,2,4-triazin-4-yl]acetamide 
• 1441160-71-9 3-(3-benzyloxy-2-oxopropyl)-5-methyl-1,3,4-oxadiazol-2-one 
• 93950-95-9 1-benzyloxy-2-carbamoyloxy-3-(2-methoxy-phenoxy)-propane 
• 128495-88-5 (R)-2-acetoxy-1-chloro-3-benzyloxy-2-propanol 
• 99789-21-6 t-4-Acetoxy-6-benzyloxymethyl-r-2-ethoxy-3,4-dihydro-5-phenylthio-2H-pyran 
• 99789-21-6 c-4-Acetoxy-6-benzyloxymethyl-r-2-ethoxy-3,4-dihydro-5-phenylthio-2H-pyran 
• 99789-24-9 (2RS,4RS)-6-Benzyloxymethyl-2-ethoxy-3,4-dihydro-5-phenylthio-2H-pyran-4-ol 
• 99789-36-3 1-Benzyloxy-4-dimethylamino-3-phenylthio-3-buten-2-on 

Relevant articles and documents

SYNTHESIS AND UTEROSTIMULATING ACTIVITY OF DERIVATIVES OF 1-DIALKYLAMINO-3-ALKOXY-2-PROPANOL

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A phosphonium ylide as a visible light organophotoredox catalyst

A phosphonium ylide-based visible light organophotoredox catalyst has been designed and successfully applied to halohydrin synthesis using trichloroacetonitrile and epoxides. An oxidative quenching cycle by the ylide catalyst was established, which was confirmed by experimental mechanistic studies.

SULFONIMIDAMIDE COMPOUNDS AS NLRP3 MODULATORS

Described herein are compounds of Formula (I), Formula (I-A), and Formula (I-B), solvates thereof, tautomers thereof, and pharmaceutically acceptable salts of the foregoing, Further described herein are methods of inhibiting NLRP3 using said compounds, and methods of and compositions useful in treating NLRP3-dependent disorders.

Visible-light-triggered Catalytic Halohydrin Synthesis from Epoxides and Trichloroacetonitrile by Copper and Iron Salts

Preparation of vicinal halohydrins, in which copper or iron chlorides catalyze the ring-opening reaction of epoxides with visible light effectively, is described. The use of trichloroacetonitrile as a halogen source enables catalytic HCl generation under the mild conditions. This method can also be applied to the aziridine ring-opening reaction.