Cas 106873-06-7,((4S,5R,6R)-5-Benzyloxycarbonylamino-2,2-dimethyl-6-vinyl-[1,3]dioxan-4-yl)-acetic acid tert-butyl ester

106873-06-7

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Basic information

Product Name: ((4S,5R,6R)-5-Benzyloxycarbonylamino-2,2-dimethyl-6-vinyl-[1,3]dioxan-4-yl)-acetic acid tert-butyl ester
Synonyms:
CAS NO:106873-06-7
Molecular Formula:
Molecular Weight: 405.491
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: ((4S,5R,6R)-5-Benzyloxycarbonylamino-2,2-dimethyl-6-vinyl-[1,3]dioxan-4-yl)-acetic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((4S,5R,6R)-5-Benzyloxycarbonylamino-2,2-dimethyl-6-vinyl-[1,3]dioxan-4-yl)-acetic acid tert-butyl ester(106873-06-7)
EPA Substance Registry System: ((4S,5R,6R)-5-Benzyloxycarbonylamino-2,2-dimethyl-6-vinyl-[1,3]dioxan-4-yl)-acetic acid tert-butyl ester(106873-06-7)

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: 106873-06-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 106873-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106873-06:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*3)+(2*0)+(1*6)=127
127 % 10 = 7
So 106873-06-7 is a valid CAS Registry Number.

106873-06-7Upstream product

95107-95-2 ((4S,5R,6R)-5-tert-Butoxycarbonylamino-2,2-dimethyl-6-vinyl-[1,3]dioxan-4-yl)-acetic acid tert-butyl ester

106873-06-7Downstream Products

106873-06-7Relevant academic research and scientific papers

SELECTIVE TRANSFORMATION OF N-t-BUTOXYCARBONYL GROUP INTO N-ALKOXYCARBONYL GROUP via N-CARBOXYLATE ION EQUIVALENT

Sakaitani, Masahiro,Ohfune, Yasufumi

, p. 5543 - 5546 (1985)

Reaction of a variety of N-t-butoxycarbonyl compounds with t-butyldimethylsilyl trifluoromethanesulfonate afforded the N-t-butyldimethylsilyloxycarbonyl compounds, chemoselectively, which upon treatment with an alkyl or aryl halide provided the corresponding N-alkoxy- or N-aryloxycarbonyl compounds, efficiently.

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