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14548-60-8

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14548-60-8 Usage

General Description

(Benzyloxy)methanol, also known as benzyl ether, is a chemical compound with the formula C7H8O2. It is a colorless liquid with a pleasant odor, and is commonly used as a solvent in various chemical reactions. (Benzyloxy)methanol is an important intermediate in the production of pharmaceuticals, dyes, and perfumes. It is also used as a fragrance ingredient in cosmetic and personal care products. The compound is known to be flammable and should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 14548-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14548-60:
(7*1)+(6*4)+(5*5)+(4*4)+(3*8)+(2*6)+(1*0)=108
108 % 10 = 8
So 14548-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2/c9-7-10-6-8-4-2-1-3-5-8/h1-5,9H,6-7H2

14548-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name phenylmethoxymethanol

1.2 Other means of identification

Product number -
Other names benzyloxymethol

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:14548-60-8 SDS

14548-60-8Downstream Products

14548-60-8Relevant articles and documents

Lewis Base–Br?nsted Acid–Enzyme Catalysis in Enantioselective Multistep One-Pot Syntheses

Giesler, Markus,Guder, Marian,Hartmann, Laura,Mantel, Marvin,Pietruszka, J?rg,Rüthlein, Elisabeth

supporting information, p. 16700 - 16706 (2021/05/07)

Establishing one-pot, multi-step protocols combining different types of catalysts is one important goal for increasing efficiency in modern organic synthesis. In particular, the high potential of biocatalysts still needs to be harvested. Based on an in-depth mechanistic investigation of a new organocatalytic protocol employing two catalysts {1,4-diazabicyclo[2.2.2]octane (DABCO); benzoic acid (BzOH)}, a sequence was established providing starting materials for enzymatic refinement (ene reductase; alcohol dehydrogenase): A gram-scale access to a variety of enantiopure key building blocks for natural product syntheses was enabled utilizing up to six catalytic steps within the same reaction vessel.

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