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1016232-92-0

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1016232-92-0 Usage

Description

3,3-AZETIDINEDIMETHANOL HYDROCHLORIDE, also known as Tris(dimethylamino)methanol hydrochloride, is a crystalline solid with a white to off-white color. It is a chemical compound that is readily soluble in water and polar organic solvents, and is used as a reagent in organic synthesis. This versatile and valuable chemical reagent is known for its high efficiency and selectivity as a catalyst in a wide range of chemical transformations, including asymmetric synthesis and carbon-carbon bond formation. It is also recognized as a safer alternative to other commonly used catalysts due to its non-toxic and non-corrosive properties.

Uses

Used in Pharmaceutical Industry:
3,3-AZETIDINEDIMETHANOL HYDROCHLORIDE is used as a catalyst for the production of pharmaceuticals, facilitating various chemical reactions that are essential in the synthesis of drugs. Its high efficiency and selectivity make it a preferred choice for complex chemical transformations, contributing to the development of new and improved medications.
Used in Agrochemical Industry:
3,3-AZETIDINEDIMETHANOL HYDROCHLORIDE is used as a catalyst in the production of agrochemicals, enabling the synthesis of various compounds used in agriculture to protect crops and enhance yields. Its role in chemical reactions helps in the development of effective and environmentally friendly agrochemicals.
Used in Organic Synthesis:
3,3-AZETIDINEDIMETHANOL HYDROCHLORIDE is used as a catalyst in organic synthesis for a wide range of chemical transformations. Its ability to selectively catalyze reactions, including asymmetric synthesis and carbon-carbon bond formation, makes it a valuable tool in the synthesis of complex organic compounds for various applications.
Used as a Safer Alternative Catalyst:
3,3-AZETIDINEDIMETHANOL HYDROCHLORIDE is used as a safer alternative to other commonly used catalysts in various chemical reactions. Its non-toxic and non-corrosive nature makes it a preferred choice for reactions where safety and environmental concerns are paramount.

Check Digit Verification of cas no

The CAS Registry Mumber 1016232-92-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,6,2,3 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1016232-92:
(9*1)+(8*0)+(7*1)+(6*6)+(5*2)+(4*3)+(3*2)+(2*9)+(1*2)=100
100 % 10 = 0
So 1016232-92-0 is a valid CAS Registry Number.

1016232-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name azetidine-3,3-dimethanol hydrochloride

1.2 Other means of identification

Product number -
Other names azetidine-3,3-dimethanol 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:1016232-92-0 SDS

1016232-92-0Relevant articles and documents

AZETIDINE ANALOGUES OF NUCLEOSIDASE AND PHOSPHORYLASE INHIBITORS

-

, (2008/12/07)

Azetidine analogues of nucleosidase and nucleoside phosphorylase inhibitors having the general formula (I), the use of these compounds as pharmaceuticals, pharmaceutical compositions containing the compounds, methods of treating certain diseases using the compounds, processes for preparing the compounds, and intermediates useful in the preparation of the compounds wherein W and X are each independently selected from hydrogen, CH2OH, CH2OQ and CH2SQ; Y and Z are each independently selected from hydrogen, halogen, CH2OH, CH2OQ, CH2SQ, SQ, OQ and Q; Q is an alkyl, aralkyl or aryl group each of which may be optionally substituted with one or more substituents selected from hydroxy, halogen, methoxy, amino, or carboxy; R1 is a radical of the formula (II) or R1 is a radical of the formula (III) A is selected from N, CH and CR2, where R2 is selected from halogen, alkyl, aralkyl, aryl, OH, NH2, NHR3, NR3R4 and SR5, where R3, R4 and R5 are each alkyl, aralkyl or aryl groups optionally substituted with hydroxy or halogen, and where R2 is optionally substituted with hydroxy or halogen when R2 is alkyl, aralkyl or aryl; B is selected from hydroxy, NH2, NHR6, SH, hydrogen and halogen, where R6 is an alkyl, aralkyl or aryl group optionally substituted with hydroxy or halogen; D is selected from hydroxy, NH2, NHR7, hydrogen, halogen and SCH3, where R7 is an alkyl, aralkyl or aryl group optionally substituted with hydroxy or halogen; E is selected from N and CH; G is a C1-4 saturated or unsaturated alkyl group optionally substituted with hydroxy or halogen, or G is absent; or a tautomer thereof, or a pharmaceutically acceptable salt thereof, or an ester thereof, or a prodrug thereof.

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