Cas 16606-18-1,1,3,2-Diazaphospholidine, 1,2,3-trimethyl-, 2-oxide

16606-18-1

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Basic information

Product Name: 1,3,2-Diazaphospholidine, 1,2,3-trimethyl-, 2-oxide
Synonyms: 1,2,3-trimethyl-1,3,2;1,3,2-Diazaphospholidine,1,2,3-trimethyl-,2-oxide;1,2,3-trimethyl-[1,3,2]diazaphospholidine 2-oxide;1,2,3-Trimethyl-2-oxo-1,3,2-diazaphospholidin;1,2,3-Trimethyltetrahydro-1,3,2-diazaphosphole 2-oxide;1,3,2-diazaphospholidine-2-methyl-1,3-dimethyl 2-oxide;
CAS NO:16606-18-1
Molecular Formula: C5H13N2OP
Molecular Weight: 148.145
EINECS: N/A
Product Categories: N/A
Mol File: 16606-18-1.mol

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: 1,3,2-Diazaphospholidine, 1,2,3-trimethyl-, 2-oxide(CAS DataBase Reference)
NIST Chemistry Reference: 1,3,2-Diazaphospholidine, 1,2,3-trimethyl-, 2-oxide(16606-18-1)
EPA Substance Registry System: 1,3,2-Diazaphospholidine, 1,2,3-trimethyl-, 2-oxide(16606-18-1)

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: 16606-18-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 16606-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,0 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16606-18:
(7*1)+(6*6)+(5*6)+(4*0)+(3*6)+(2*1)+(1*8)=101
101 % 10 = 1
So 16606-18-1 is a valid CAS Registry Number.

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16606-18-1Relevant academic research and scientific papers

A divergent synthesis of minor groove binders with tail group variation

Breen, David,Kennedy, Alan R.,Suckling, Colin J.

experimental part, p. 178 - 186 (2009/04/07)

A new synthesis of polyamide minor groove binders in which diversity is introduced by the nucleophilic substitution of a 2-sulfido-1,3,2- diazaphospholidinyloxy substituent by volatile secondary amine nucleophiles is described. Such a method has potential

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