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chlorobromofosfamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146367-82-0

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146367-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146367-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,6 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 146367-82:
(8*1)+(7*4)+(6*6)+(5*3)+(4*6)+(3*7)+(2*8)+(1*2)=150
150 % 10 = 0
So 146367-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H15BrClN2O2P/c8-2-6-11-5-1-7-13-14(11,12)10-4-3-9/h1-7H2,(H,10,12)

146367-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-bromoethyl)-N-(2-chloroethyl)-2-oxo-1,3,2λ<sup>5</sup>-oxazaphosphinan-2-amine

1.2 Other means of identification

Product number -
Other names Chlorobromofosfamide

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:146367-82-0 SDS

146367-82-0Downstream Products

146367-82-0Relevant academic research and scientific papers

Process for the production of 1,3,2-oxazaphosphorinanes

-

, (2008/06/13)

Process for production of derivatives of 1,3,2-oxazaphosphorinane of general formula 1, STR1 wherein R1 and R2 represent hydrogen atom or 2-halogenoalkyl group, and R1 and R2 are not at the same time hydrogen atoms, and X represents halogen atom is based, according to the invention, on the reduction of the respective 3-halogenoacyl derivatives of 1,3,2-oxazaphosphorinane of general formula 2, STR2 wherein the substituents have the above given meaning. The reduction is accomplished with the use of sodium borohydride in the presence of boron trifluoride etherate. Derivatives that are prepared by the procedure described here demonstrate antitumor activity.

Process for the production of 2-(2-halogenoethylamino)-2-oxo-3-(2-halogenoethyl)-1.3.2.-oxazaphosphorinanes

-

, (2008/06/13)

Process for production of racemic or enantiomeric form of 2-(2-halogenoethylamino)-2-oxo-3-(2-halogenoethyl)-1.3.2.-oxazaphosphorinanes of general formula 1, STR1 wherein X and Y are the same or different and represent halogen atoms is based, according to invention, on the reaction of enantiomeric or racemic form of ethyleneimide of general formula 2, STR2 wherein Y is the same as above, with aqueous solution of hydrogen halide. Compounds of general formula 1, where X and Y are different and represent halogen atoms, possess better antileukemic activity than ifosfamide.

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