Cas 700828-06-4,2-methyl-propane-2-sulfinic acid (4-<i>tert</i>-butyl-cyclohexylidene)-amide

700828-06-4

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Basic information

Product Name: 2-methyl-propane-2-sulfinic acid (4-tert-butyl-cyclohexylidene)-amide
Synonyms: 2-methyl-propane-2-sulfinic acid (4-tert-butyl-cyclohexylidene)-amide
CAS NO:700828-06-4
Molecular Formula:
Molecular Weight: 257.44
EINECS: N/A
Product Categories: N/A
Mol File: 700828-06-4.mol
Article Data: 1

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: 2-methyl-propane-2-sulfinic acid (4-tert-butyl-cyclohexylidene)-amide(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-propane-2-sulfinic acid (4-tert-butyl-cyclohexylidene)-amide(700828-06-4)
EPA Substance Registry System: 2-methyl-propane-2-sulfinic acid (4-tert-butyl-cyclohexylidene)-amide(700828-06-4)

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: 700828-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 700828-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,8,2 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 700828-06:
(8*7)+(7*0)+(6*0)+(5*8)+(4*2)+(3*8)+(2*0)+(1*6)=134
134 % 10 = 4
So 700828-06-4 is a valid CAS Registry Number.

700828-06-4Upstream product

700828-06-4Downstream Products

700828-06-4Relevant articles and documents

Highly stereoselective addition of organometallic reagents to N-tert-butanesulfinyl imines derived from 3- and 4-substituted cyclohexanones

McMahon, Jeffrey P.,Ellman, Jonathan A.

, p. 1645 - 1647 (2007/10/03)

Addition of alkyl or aryl Grignard reagents to N-sulfinyl imines derived from 3- and 4-substituted cyclohexanones proceeds with good yields and with excellent diasteroselectivity. The selectivity of the reaction is controlled by the ring substituent rathe

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