1218-65-1

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Basic information

Product Name: bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate
Synonyms: bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate;Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (bicyclo[2.2.1]hept-5-en-2-yl)methyl ester
CAS NO:1218-65-1
Molecular Formula: C16H20O2
Molecular Weight: 244.3288
EINECS: 214-938-5
Product Categories: N/A
Mol File: 1218-65-1.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: 337.1°Cat760mmHg
Flash Point: 151°C
Appearance: /
Density: 1.159g/cm³
Vapor Pressure: 0.000108mmHg at 25°C
Refractive Index: 1.567
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate(1218-65-1)
EPA Substance Registry System: bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate(1218-65-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1218-65-1(Hazardous Substances Data)

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Bicyclo[2.2.1]hept-5-ene-2-carboxylicacid, bicyclo[2.2.1]hept-5-en-2-ylmethyl ester
Cas No: 1218-65-1
No Data
10 Gram
500 Kilogram/Month
Zibo Hangyu Biotechnology Development Co., Ltd
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6-bicyclo[2.2.1]hept-2-enylmethyl bicyclo[2.2.1]hept-2-ene-6-carboxylate
Cas No: 1218-65-1
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BOC Sciences
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Bicyclo[2.2.1]hept-5-ene-2-carboxylicacid, bicyclo[2.2.1]hept-5-en-2-ylmethyl ester
Cas No: 1218-65-1
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Antimex Chemical Limied
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Bicyclo[2.2.1]hept-5-ene-2-carboxylicacid, bicyclo[2.2.1]hept-5-en-2-ylmethyl ester
Cas No: 1218-65-1
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Chemlyte Solutions
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bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate
Cas No: 1218-65-1
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Shanghai Run-Biotech Co., Ltd.
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Bicyclo[2.2.1]hept-5-ene-2-carboxylicacid, bicyclo[2.2.1]hept-5-en-2-ylmethyl ester
Cas No: 1218-65-1
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CHEMOS GmbH
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1218-65-1 Usage

General Description

Bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate is a chemical compound with a bicyclic structure that contains two adjacent seven-membered rings. It is commonly used in the field of organic chemistry as a building block or intermediate in the synthesis of various compounds. The compound has a double bond and a carboxylic acid ester functional group, which makes it versatile for use in reactions such as hydrogenation, hydrolysis, and acylation. Its unique structure and reactivity make it valuable for the creation of complex organic molecules in pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1218-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1218-65:
(6*1)+(5*2)+(4*1)+(3*8)+(2*6)+(1*5)=61
61 % 10 = 1
So 1218-65-1 is a valid CAS Registry Number.

InChI:InChI=1/C16H20O2/c17-16(15-8-11-2-4-13(15)6-11)18-9-14-7-10-1-3-12(14)5-10/h1-4,10-15H,5-9H2

1218-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	5-bicyclo[2.2.1]hept-2-enylmethyl bicyclo[2.2.1]hept-2-ene-5-carboxylate

1.2 Other means of identification

Product number	-
Other names	EINECS 214-938-5

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:1218-65-1 SDS

1218-65-1Upstream product

1218-65-1Downstream Products

1218-65-1Relevant articles and documents

Medved,Christie

, p. 240 (1964)

Reactions of Norbornyl Aldehydes with Diiron Nonacarbonyl: A Stereoselective Pathway to "Geminal-Faced" Esters and Alcohols

Bankston, Donald

, p. 2003 - 2006 (2007/10/02)

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