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770-70-7

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Description

1-(Chloromethyl)adamantane, also known as adamantyl chloromethyl ether or amantadine, is a chemical compound with the molecular formula C11H17Cl. It is a chloromethyl derivative of adamantane, a type of diamondoid hydrocarbon with a unique structure. 1-(CHLOROMETHYL)ADAMANTANE is characterized by its unique adamantane framework and a reactive chloromethyl group, which makes it a versatile building block in various chemical reactions and applications.

Uses

Used in Organic Synthesis:
1-(Chloromethyl)adamantane is used as a building block in organic synthesis for the creation of various organic compounds. Its adamantane structure provides stability and rigidity, while the chloromethyl group allows for further functionalization and the formation of new chemical bonds.
Used in Pharmaceutical Production:
1-(Chloromethyl)adamantane serves as a precursor in the production of pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs, potentially leading to the discovery of novel therapeutic agents.
Used in Materials Science:
In the field of materials science, 1-(Chloromethyl)adamantane can be utilized to develop new materials with specific properties. Its adamantane core and reactive chloromethyl group can be exploited to create materials with tailored characteristics for various applications.
Used in Chemical Research:
1-(Chloromethyl)adamantane is a valuable compound for chemical research, as it can be used to study the properties and reactivity of adamantane derivatives. This knowledge can contribute to the understanding of diamondoid hydrocarbons and their potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 770-70-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 770-70:
(5*7)+(4*7)+(3*0)+(2*7)+(1*0)=77
77 % 10 = 7
So 770-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H17Cl/c12-7-11-4-8-1-9(5-11)3-10(2-8)6-11/h8-10H,1-7H2

770-70-7SDS

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 1-(chloromethyl)adamantane

1.2 Other means of identification

Product number -
Other names 1-adamantyl methyl chloride

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:770-70-7 SDS

770-70-7Downstream Products

770-70-7Relevant articles and documents

Solvent-equilibrated ion pairs from carbene fragmentation reactions

Moss, Robert A.,Zheng, Fengmei,Fede, Jean-Marie,Johnson, Lauren A.,Sauers, Ronald R.

, p. 12421 - 12431 (2007/10/03)

[R+ OC Cl-] ion pairs were generated in methanol/dichloroethane solutions, with R+ as the 1-bicyclo[2.2.2]octyl, 1-adamantyl, or 3-homoadamantyl cation. Ion pairs were produced either by the direct fragmentation of alkoxychlorocarbenes (ROCCl), with R = 1-bicyclo[2.2.2]octyl, 1-adamantyl, or 3-homoadamantyl, or by the ring expansion-fragmentation of R′CH2OCCl, with R′ = 1-norbornyl, 3-noradamantyl, or 1-adamantyl. Correlations of the [ROMe]/[RCl] product ratios as a function of the mole fraction of MeOH in dichloroethane showed that the homoadamantyl chloride ion pairs, produced by either the direct or ring expansion-fragmentations, were identical, solvent- and anion -equilibrated, and precursor independent. Laser flash photolysis experiments gave 20-30 ps as the time required for solvent equilibration and precursor independence. Methanol/chloride selectivities of the (less-stable) 1-adamantyl chloride and 1-bicyclo[2.2.2]octyl chloride ion pairs were not independent of their ROCCl or R′CH2OCCl precursors. Computational studies provided transition states for the fragmentations and for the structures of the ion pairs.

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