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Benzenemethanol, a-[(1S)-1-aminoethyl]-, hydrochloride (1:1), (aS)-rel- is a chemical compound with the molecular formula C8H13NO·HCl. It is a derivative of benzyl alcohol, featuring an aminoethyl group attached to the alpha position (adjacent to the hydroxyl group). The compound is a chiral molecule, with the (1S) configuration indicating that the amino group is on the same side of the molecule as the hydroxyl group when viewed along the bond connecting the benzene ring to the chiral carbon. The hydrochloride salt form of Benzenemethanol, a-[(1S)-1-aminoethyl]-,hydrochloride (1:1), (aS)-rel- is a white crystalline solid, which is often used to improve the solubility and stability of the compound in various pharmaceutical applications. It is important to note that the specific name provided suggests a particular enantiomeric form, which is the (aS)-rel- configuration, indicating the relative arrangement of the atoms in the molecule. Benzenemethanol, a-[(1S)-1-aminoethyl]-,hydrochloride (1:1), (aS)-rel- is used in the synthesis of various pharmaceuticals and as an intermediate in organic chemistry.

1485-15-0

1485-15-0 Suppliers

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1485-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1485-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1485-15:
(6*1)+(5*4)+(4*8)+(3*5)+(2*1)+(1*5)=80
80 % 10 = 0
So 1485-15-0 is a valid CAS Registry Number.

1485-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-1-[(2R)-2-aminopropyl]cyclohexa-2,4-dien-1-ol,hydrochloride

1.2 Other means of identification

Product number -
Other names (1RS,2RS)-2-amino-1-phenyl-propan-1-ol,hydrochloride

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:1485-15-0 SDS

1485-15-0Relevant academic research and scientific papers

Simple preparation process of syn phenylpropanolamines from racemic O-TBDPS cyanohydrins

Li, Qing-Lan,Tang, Shi,Zhou, Dong,Tang, Xin-Mei

, p. 1600 - 1607 (2014/06/09)

In this article, a practically interesting route for the diastereoselective synthesis of phenylpropanolamines has been demonstrated for the first time. Using racemic O-tert-butyldiphenylsilyl (TBDPS) cyanohydrins as the starting materials, various syn phenylpropanolamines and derivatives (e.g., norpseudophedrine) have been successfully prepared in exellent diastereoselectivity via a practically interesting process.

STEREOCHEMICAL COURSE OF THE REACTION OF 2-HALOETHYL ISOTHIOCYANATES WITH NUCLEOPHILES. sTEREOSPECIFIC ROUTE TO 4,5-DISUBSTITUTED Δ2-THIAZOLINES AND THIAZOLIDINE-2-THIONES

Kniezo, Ladislav,Kristian, Pavol,Budesinsky, Milos,Havrilova, Katarina

, p. 717 - 728 (2007/10/02)

Diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes have been prepared.They reacted stereospecifically with CH3ONa, diethylamine, aniline and NaSH to give pure cis or trans-4,5-disubstituted Δ2-thiazolines and thiazolidine-2-thiones whose configuration was determined using the nuclear Overhauser effect.The preponderant conformation of diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes was estimated on the basis of coupling constants of vicinal protons.