Basic information

Product Name: (R)-3-(2,2,2-Trichloro-ethoxycarbonylamino)-hex-5-enoic acid
Synonyms:
CAS NO:82448-91-7
Molecular Formula:
Molecular Weight: 304.558
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (R)-3-(2,2,2-Trichloro-ethoxycarbonylamino)-hex-5-enoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-(2,2,2-Trichloro-ethoxycarbonylamino)-hex-5-enoic acid(82448-91-7)
EPA Substance Registry System: (R)-3-(2,2,2-Trichloro-ethoxycarbonylamino)-hex-5-enoic acid(82448-91-7)

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: 82448-91-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82448-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,4 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82448-91:
(7*8)+(6*2)+(5*4)+(4*4)+(3*8)+(2*9)+(1*1)=147
147 % 10 = 7
So 82448-91-7 is a valid CAS Registry Number.

82448-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	(R)-3-(((2,2,2-trichloroethoxy)carbonyl)amino)hex-5-enoic acid

1.2 Other means of identification

Product number	-
Other names	-

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:82448-91-7 SDS

82448-91-7Upstream product

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82448-91-7Relevant academic research and scientific papers

AN ENANTIOSELECTIVE ROUTE TO AN INTERMEDIATE OF THE CARBAPENAM SYSTEM FROM THE CHIRAL γ-BUTYROLACTONE

Takano, Seiichi,Kasahara, Chiyoshi,Ogasawara, Kunio

, p. 631 - 634 (1982)

A new enantioselective synthesis of the keto ester(16) containing β-lactam ring system has been developed using the chiral lactone(1) as a starting material.

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